Skip to content
← Back to this collection

LABELS · c48edbf8-425f-4e11-8892-467e868d9fba

ZOLADEX

Open original source → · Download preserved record

Preserved label snapshot, not confirmation of a current approved indication. Approval/withdrawal status must be checked for the exact disease, setting and regimen.

Label effective date
2026-03-24
Captured
2026-09-09T23:37:58.719708+00:00
Current indication reconciliation
Not reconciled

Indications and usage: exact source text

  1. 1 INDICATIONS AND USAGE ZOLADEX is a Gonadotropin Releasing Hormone (GnRH) agonist indicated for: Use in combination with flutamide for the management of locally confined carcinoma of the prostate ( 1.1 ) Palliative treatment of advanced carcinoma of the prostate ( 1.2 ) The management of endometriosis ( 1.3 ) Use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding ( 1.4 ) Use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women ( 1.5 ) 1.1 Stage B2-C Prostatic Carcinoma ZOLADEX is indicated for use in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate. Treatment with ZOLADEX and flutamide should start 8 weeks prior to initiating radiation therapy and continue during radiation therapy [see Dosage and Administration ( 2.1 ) and Clinical Studies ( 14.1 )]. 1.2 Prostatic Carcinoma ZOLADEX is indicated in the palliative treatment of advanced carcinoma of the prostate [see Dosage and Administration ( 2.2 ) and Clinical Studies ( 14.2 )]. 1.3 Endometriosis ZOLADEX is indicated for the management of endometriosis, including pain relief and reduction of endometriotic lesions for the duration of therapy. Experience with ZOLADEX for the management of endometriosis has been limited to women 18 years of age and older treated for 6 months [see Dosage and Administration ( 2.3 ) and Clinical Studies ( 14.3 )]. 1.4 Endometrial Thinning ZOLADEX is indicated for use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding [see Dosage and Administration ( 2.4 ) and Clinical Studies ( 14.4 )]. 1.5 Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women. The estrogen and progesterone receptor values may help to predict whether ZOLADEX therapy is likely to be beneficial [see Dosage and Administration ( 2.5 ), Clinical Pharmacology ( 12.1 ), and Clinical Studies ( 14.5 )]. The automatic safety feature of the syringe aids in the prevention of needlestick injury.
Full extracted label fields
application numbers
  1. NDA019726
boxed warning exact
    brand names
    1. ZOLADEX
    current indication status
    not_reconciled
    dailymed set url
    https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=294b168b-6e5f-4db9-bf70-d599271458b3
    generic names
    1. GOSERELIN
    id
    c48edbf8-425f-4e11-8892-467e868d9fba
    indications and usage exact
    1. 1 INDICATIONS AND USAGE ZOLADEX is a Gonadotropin Releasing Hormone (GnRH) agonist indicated for: Use in combination with flutamide for the management of locally confined carcinoma of the prostate ( 1.1 ) Palliative treatment of advanced carcinoma of the prostate ( 1.2 ) The management of endometriosis ( 1.3 ) Use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding ( 1.4 ) Use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women ( 1.5 ) 1.1 Stage B2-C Prostatic Carcinoma ZOLADEX is indicated for use in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate. Treatment with ZOLADEX and flutamide should start 8 weeks prior to initiating radiation therapy and continue during radiation therapy [see Dosage and Administration ( 2.1 ) and Clinical Studies ( 14.1 )]. 1.2 Prostatic Carcinoma ZOLADEX is indicated in the palliative treatment of advanced carcinoma of the prostate [see Dosage and Administration ( 2.2 ) and Clinical Studies ( 14.2 )]. 1.3 Endometriosis ZOLADEX is indicated for the management of endometriosis, including pain relief and reduction of endometriotic lesions for the duration of therapy. Experience with ZOLADEX for the management of endometriosis has been limited to women 18 years of age and older treated for 6 months [see Dosage and Administration ( 2.3 ) and Clinical Studies ( 14.3 )]. 1.4 Endometrial Thinning ZOLADEX is indicated for use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding [see Dosage and Administration ( 2.4 ) and Clinical Studies ( 14.4 )]. 1.5 Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women. The estrogen and progesterone receptor values may help to predict whether ZOLADEX therapy is likely to be beneficial [see Dosage and Administration ( 2.5 ), Clinical Pharmacology ( 12.1 ), and Clinical Studies ( 14.5 )]. The automatic safety feature of the syringe aids in the prevention of needlestick injury.
    indications and usage tables exact
      is original packager
      1. true
      manufacturer names
      1. TerSera Therapeutics LLC
      matched search terms
      1. cancer
      2. carcinoma
      package ndcs
      1. 70720-950-36
      product ndcs
      1. 70720-950
      product types
      1. HUMAN PRESCRIPTION DRUG
      recent major changes exact
      1. Warnings and Precautions ( 5.7 ) 9/2025
      record type
      complete_spl_indications_section_candidate
      routes
      1. SUBCUTANEOUS
      rxcuis
      1. 105641
      2. 310592
      source batch
      file
      /private/tmp/cancer-full-research/indications/raw/labels-00600.json
      meta
      disclaimer
      Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
      last updated
      2026-09-09
      results
      limit
      100
      skip
      600
      total
      830
      sha256
      a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
      url
      https://api.fda.gov/drug/label.json?search=%28indications_and_usage%3Acancer+OR+indications_and_usage%3Acarcinoma+OR+indications_and_usage%3Acarcinomas+OR+indications_and_usage%3Alymphoma+OR+indications_and_usage%3Alymphomas+OR+indications_and_usage%3Aleukemia+OR+indications_and_usage%3Aleukaemia+OR+indications_and_usage%3Asarcoma+OR+indications_and_usage%3Asarcomas+OR+indications_and_usage%3Amelanoma+OR+indications_and_usage%3Amyeloma+OR+indications_and_usage%3Atumor+OR+indications_and_usage%3Atumors+OR+indications_and_usage%3Atumour+OR+indications_and_usage%3Atumours+OR+indications_and_usage%3Aneoplasm+OR+indications_and_usage%3Aneoplasms+OR+indications_and_usage%3Amalignant+OR+indications_and_usage%3Amalignancy+OR+indications_and_usage%3Amyelodysplastic+OR+indications_and_usage%3Amyelofibrosis+OR+indications_and_usage%3Amastocytosis+OR+indications_and_usage%3Aglioma+OR+indications_and_usage%3Aglioblastoma+OR+indications_and_usage%3Aneuroblastoma+OR+indications_and_usage%3Aretinoblastoma+OR+indications_and_usage%3Apheochromocytoma+OR+indications_and_usage%3Aparaganglioma+OR+indications_and_usage%3Amyeloproliferative+OR+indications_and_usage%3Awaldenstrom+OR+indications_and_usage%3Apolycythemia+OR+indications_and_usage%3Athrombocythemia+OR+indications_and_usage%3Adesmoid+OR+indications_and_usage%3Aneurofibromatosis+OR+indications_and_usage%3Ahistiocytosis%29+AND+%28openfda.application_number%3ANDA%2A+OR+openfda.application_number%3ABLA%2A%29&limit=100&skip=600&sort=id%3Aasc
      source url
      https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
      spl effective date
      2026-03-24
      spl effective time
      20260324
      spl set id
      294b168b-6e5f-4db9-bf70-d599271458b3
      spl version
      9
      substance names
      1. GOSERELIN ACETATE
      uniis
      1. 6YUU2PV0U8
      verification flags
      1. oncology_keyword_candidate_not_clinically_classified
      2. spl_text_not_verified_identical_to_latest_approved_label
      3. individual_indications_not_split_or_reconciled
      4. fda_label_posted_after_spl_effective_date_requires_version_review
      Drugs@FDA application source records
      1. application number
        NDA019726
        payload
        all indexed label documents
        1. Appl No
          019726
          Application Docs Date
          2009-09-17 00:00:00
          Application Docs ID
          11653
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          50
          Submission Type
          SUPPL
        2. Appl No
          019726
          Application Docs Date
          2009-09-17 00:00:00
          Application Docs ID
          11654
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          51
          Submission Type
          SUPPL
        3. Appl No
          019726
          Application Docs Date
          2011-01-20 00:00:00
          Application Docs ID
          11655
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          54
          Submission Type
          SUPPL
        4. Appl No
          019726
          Application Docs Date
          2013-06-17 00:00:00
          Application Docs ID
          11656
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          56
          Submission Type
          SUPPL
        5. Appl No
          019726
          Application Docs Date
          2015-02-13 00:00:00
          Application Docs ID
          11657
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          59
          Submission Type
          SUPPL
        6. Appl No
          019726
          Application Docs Date
          1998-07-27 00:00:00
          Application Docs ID
          33888
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          24
          Submission Type
          SUPPL
        7. Appl No
          019726
          Application Docs Date
          2009-09-17 00:00:00
          Application Docs ID
          33889
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          52
          Submission Type
          SUPPL
        8. Appl No
          019726
          Application Docs Date
          2013-06-17 00:00:00
          Application Docs ID
          33890
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          57
          Submission Type
          SUPPL
        9. Appl No
          019726
          Application Docs Date
          2014-10-09 00:00:00
          Application Docs ID
          33891
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          58
          Submission Type
          SUPPL
        10. Appl No
          019726
          Application Docs Date
          2023-03-17 00:00:00
          Application Docs ID
          73789
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          69
          Submission Type
          SUPPL
        11. Appl No
          019726
          Application Docs Date
          2025-09-30 00:00:00
          Application Docs ID
          83587
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          74
          Submission Type
          SUPPL
        12. Appl No
          019726
          Application Docs Date
          2026-05-12 00:00:00
          Application Docs ID
          85883
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          76
          Submission Type
          SUPPL
        all submission records
        1. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          76
          Submission Status
          AP
          Submission Status Date
          2026-05-06 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        2. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          74
          Submission Status
          AP
          Submission Status Date
          2025-09-23 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        3. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          69
          Submission Status
          AP
          Submission Status Date
          2023-03-16 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        4. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          66
          Submission Status
          AP
          Submission Status Date
          2021-06-17 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        5. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          4
          Submission No
          60
          Submission Status
          AP
          Submission Status Date
          2016-07-19 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        6. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          59
          Submission Status
          AP
          Submission Status Date
          2015-02-12 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        7. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          58
          Submission Status
          AP
          Submission Status Date
          2014-10-07 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        8. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          57
          Submission Status
          AP
          Submission Status Date
          2013-06-18 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        9. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          56
          Submission Status
          AP
          Submission Status Date
          2013-06-18 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        10. Appl No
          019726
          Review Priority
          901 REQUIRED
          Submission Class Code ID
          3
          Submission No
          54
          Submission Status
          AP
          Submission Status Date
          2011-01-14 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        11. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          52
          Submission Status
          AP
          Submission Status Date
          2009-08-31 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        12. Appl No
          019726
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          51
          Submission Status
          AP
          Submission Status Date
          2009-08-31 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        application number
        NDA019726
        approval interpretation
        Application linkage and approved submission are not indication-level current approval verification
        current indication status
        not_reconciled
        has approved submission record
        true
        latest approved submission date
        2026-05-06
        latest label selection rule
        max FDA ApplicationDocsDate, including all ties; posting date is not approval date and latest indexed document may be incomplete
        latest posted label documents
        1. Appl No
          019726
          Application Docs Date
          2026-05-12 00:00:00
          Application Docs ID
          85883
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          76
          Submission Type
          SUPPL
        official application record
        Appl No
        019726
        Appl Public Notes
        Appl Type
        NDA
        Sponsor Name
        TERSERA
        openfda application present
        true
        products
        1. Active Ingredient
          GOSERELIN ACETATE
          Appl No
          019726
          Drug Name
          ZOLADEX
          Form
          IMPLANT;IMPLANTATION
          Product No
          001
          Reference Drug
          1
          Reference Standard
          1
          Strength
          EQ 3.6MG BASE
          marketing status
          1. Prescription

      Source passages and status connections

      Passage classifications are automated and are not treatment recommendations. Connections apply only to their recorded indication scope.

      Passage 1 · positive indication candidate
      application numbers
      1. NDA019726
      brand names
      1. ZOLADEX
      classification reasons
      1. explicit_positive_indication_predicate
      2. tumor_or_malignant_hematology_words_in_positive_statement
      clinical review status
      pending
      content role
      positive_indication_candidate
      context span
      end
      720
      end exclusive
      true
      exact text
      1 INDICATIONS AND USAGE ZOLADEX is a Gonadotropin Releasing Hormone (GnRH) agonist indicated for: Use in combination with flutamide for the management of locally confined carcinoma of the prostate ( 1.1 ) Palliative treatment of advanced carcinoma of the prostate ( 1.2 ) The management of endometriosis ( 1.3 ) Use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding ( 1.4 ) Use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women ( 1.5 ) 1.1 Stage B2-C Prostatic Carcinoma ZOLADEX is indicated for use in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate. Treatment wit
      label id
      c48edbf8-425f-4e11-8892-467e868d9fba
      offset unit
      unicode_code_points
      source array index
      0
      source field
      indications_and_usage_exact
      source text sha256
      f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
      start
      0
      current approval status
      not_reconciled
      duplicate text group
      dup-89063086b74fc7ccb106
      extraction review status
      automated_candidate_pending_source_review
      generic names
      1. GOSERELIN
      id
      ind-span-92a8700884b9ee327a81
      label id
      c48edbf8-425f-4e11-8892-467e868d9fba
      positive predicate support span
      end
      92
      end exclusive
      true
      exact text
      is a Gonadotropin Releasing Hormone (GnRH) agonist indicated
      label id
      c48edbf8-425f-4e11-8892-467e868d9fba
      offset unit
      unicode_code_points
      source array index
      0
      source field
      indications_and_usage_exact
      source text sha256
      f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
      start
      32
      qualifier mentions
      1. context exact
        d carcinoma of the prostate ( 1.1 ) Palliative treatment of advanced carcinoma of the prostate ( 1.2 ) The management of endometriosis ( 1.3 ) Use as an endom
        kind
        stage_or_setting
        polarity
        not_inferred
        span
        end
        267
        end exclusive
        true
        exact text
        advanced carcinoma of the prostate ( 1
        label id
        c48edbf8-425f-4e11-8892-467e868d9fba
        offset unit
        unicode_code_points
        source array index
        0
        source field
        indications_and_usage_exact
        source text sha256
        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
        start
        229
      2. context exact
        uterine bleeding ( 1.4 ) Use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women ( 1.5 )
        kind
        stage_or_setting
        polarity
        not_inferred
        span
        end
        500
        end exclusive
        true
        exact text
        advanced breast cancer in pre- and perimeno
        label id
        c48edbf8-425f-4e11-8892-467e868d9fba
        offset unit
        unicode_code_points
        source array index
        0
        source field
        indications_and_usage_exact
        source text sha256
        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
        start
        457
      3. context exact
        otropin Releasing Hormone (GnRH) agonist indicated for: Use in combination with flutamide for the management of locally confined carcinoma of the prostate ( 1.1 ) Palliative treatment of advanced carcinoma of the prost
        kind
        regimen
        polarity
        not_inferred
        span
        end
        200
        end exclusive
        true
        exact text
        in combination with flutamide for the management of locally confined carcinoma of the prostate ( 1
        label id
        c48edbf8-425f-4e11-8892-467e868d9fba
        offset unit
        unicode_code_points
        source array index
        0
        source field
        indications_and_usage_exact
        source text sha256
        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
        start
        102
      regulatory links
        schema version
        0.1.0
        source batch sha256
        a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
        source defined aliases
          source span
          end
          520
          end exclusive
          true
          exact text
          1 INDICATIONS AND USAGE ZOLADEX is a Gonadotropin Releasing Hormone (GnRH) agonist indicated for: Use in combination with flutamide for the management of locally confined carcinoma of the prostate ( 1.1 ) Palliative treatment of advanced carcinoma of the prostate ( 1.2 ) The management of endometriosis ( 1.3 ) Use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding ( 1.4 ) Use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women ( 1.5 )
          label id
          c48edbf8-425f-4e11-8892-467e868d9fba
          offset unit
          unicode_code_points
          source array index
          0
          source field
          indications_and_usage_exact
          source text sha256
          f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
          start
          0
          source url
          https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
          spl effective date
          2026-03-24
          spl set id
          294b168b-6e5f-4db9-bf70-d599271458b3
          spl version
          9
          structured fields status
          not_extracted_no_values_inferred_from_mentions
          structured indication
          age
          Source null
          approval pathway
          Source null
          biomarker and test
          Source null
          disease stage
          Source null
          limitations
          Source null
          line
          Source null
          prior therapy
          Source null
          regimen
          Source null
          tumor histology
          Source null
          use intent
          tumor_directed_candidate
          Passage 2 · positive indication candidate
          application numbers
          1. NDA019726
          brand names
          1. ZOLADEX
          classification reasons
          1. explicit_positive_indication_predicate
          2. tumor_or_malignant_hematology_words_in_positive_statement
          clinical review status
          pending
          content role
          positive_indication_candidate
          context span
          end
          906
          end exclusive
          true
          exact text
          endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding ( 1.4 ) Use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women ( 1.5 ) 1.1 Stage B2-C Prostatic Carcinoma ZOLADEX is indicated for use in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate. Treatment with ZOLADEX and flutamide should start 8 weeks prior to initiating radiation therapy and continue during radiation therapy [see Dosage and Administration ( 2.1 ) and Clinical Studies ( 14.
          label id
          c48edbf8-425f-4e11-8892-467e868d9fba
          offset unit
          unicode_code_points
          source array index
          0
          source field
          indications_and_usage_exact
          source text sha256
          f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
          start
          321
          current approval status
          not_reconciled
          duplicate text group
          dup-b54dc045a39f319c13e9
          extraction review status
          automated_candidate_pending_source_review
          generic names
          1. GOSERELIN
          id
          ind-span-4988515048c77a25c935
          label id
          c48edbf8-425f-4e11-8892-467e868d9fba
          positive predicate support span
          end
          576
          end exclusive
          true
          exact text
          is indicated
          label id
          c48edbf8-425f-4e11-8892-467e868d9fba
          offset unit
          unicode_code_points
          source array index
          0
          source field
          indications_and_usage_exact
          source text sha256
          f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
          start
          564
          qualifier mentions
          1. context exact
            Stage B2-C Prostatic Carcinoma ZOLADEX is indicated for use in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate.
            kind
            regimen
            polarity
            not_inferred
            span
            end
            705
            end exclusive
            true
            exact text
            in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate
            label id
            c48edbf8-425f-4e11-8892-467e868d9fba
            offset unit
            unicode_code_points
            source array index
            0
            source field
            indications_and_usage_exact
            source text sha256
            f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
            start
            585
          regulatory links
            schema version
            0.1.0
            source batch sha256
            a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
            source defined aliases
              source span
              end
              706
              end exclusive
              true
              exact text
              1.1 Stage B2-C Prostatic Carcinoma ZOLADEX is indicated for use in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate.
              label id
              c48edbf8-425f-4e11-8892-467e868d9fba
              offset unit
              unicode_code_points
              source array index
              0
              source field
              indications_and_usage_exact
              source text sha256
              f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
              start
              521
              source url
              https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
              spl effective date
              2026-03-24
              spl set id
              294b168b-6e5f-4db9-bf70-d599271458b3
              spl version
              9
              structured fields status
              not_extracted_no_values_inferred_from_mentions
              structured indication
              age
              Source null
              approval pathway
              Source null
              biomarker and test
              Source null
              disease stage
              Source null
              limitations
              Source null
              line
              Source null
              prior therapy
              Source null
              regimen
              Source null
              tumor histology
              Source null
              use intent
              tumor_directed_candidate
              Passage 3 · unclassified context
              application numbers
              1. NDA019726
              brand names
              1. ZOLADEX
              classification reasons
              1. no_unambiguous_positive_indication_predicate
              clinical review status
              pending
              content role
              unclassified_context
              context span
              end
              1111
              end exclusive
              true
              exact text
              women ( 1.5 ) 1.1 Stage B2-C Prostatic Carcinoma ZOLADEX is indicated for use in combination with flutamide for the management of locally confined Stage T2b-T4 (Stage B2-C) carcinoma of the prostate. Treatment with ZOLADEX and flutamide should start 8 weeks prior to initiating radiation therapy and continue during radiation therapy [see Dosage and Administration ( 2.1 ) and Clinical Studies ( 14.1 )]. 1.2 Prostatic Carcinoma ZOLADEX is indicated in the palliative treatment of advanced carcinoma of the prostate [see Dosage and Administration ( 2.2 ) and Clinical Studies ( 14.2 )]. 1.3 Endometriosis
              label id
              c48edbf8-425f-4e11-8892-467e868d9fba
              offset unit
              unicode_code_points
              source array index
              0
              source field
              indications_and_usage_exact
              source text sha256
              f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
              start
              507
              current approval status
              not_reconciled
              duplicate text group
              dup-b4b6a88c93d0dd5c3415
              extraction review status
              automated_candidate_pending_source_review
              generic names
              1. GOSERELIN
              id
              ind-span-0da6dd2cfc9e40d72f0f
              label id
              c48edbf8-425f-4e11-8892-467e868d9fba
              positive predicate support span
              Source null
              qualifier mentions
                regulatory links
                  schema version
                  0.1.0
                  source batch sha256
                  a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                  source defined aliases
                    source span
                    end
                    911
                    end exclusive
                    true
                    exact text
                    Treatment with ZOLADEX and flutamide should start 8 weeks prior to initiating radiation therapy and continue during radiation therapy [see Dosage and Administration ( 2.1 ) and Clinical Studies ( 14.1 )].
                    label id
                    c48edbf8-425f-4e11-8892-467e868d9fba
                    offset unit
                    unicode_code_points
                    source array index
                    0
                    source field
                    indications_and_usage_exact
                    source text sha256
                    f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                    start
                    707
                    source url
                    https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                    spl effective date
                    2026-03-24
                    spl set id
                    294b168b-6e5f-4db9-bf70-d599271458b3
                    spl version
                    9
                    structured fields status
                    not_extracted_no_values_inferred_from_mentions
                    structured indication
                    age
                    Source null
                    approval pathway
                    Source null
                    biomarker and test
                    Source null
                    disease stage
                    Source null
                    limitations
                    Source null
                    line
                    Source null
                    prior therapy
                    Source null
                    regimen
                    Source null
                    tumor histology
                    Source null
                    use intent
                    unclear
                    Passage 4 · positive indication candidate
                    application numbers
                    1. NDA019726
                    brand names
                    1. ZOLADEX
                    classification reasons
                    1. explicit_positive_indication_predicate
                    2. tumor_or_malignant_hematology_words_in_positive_statement
                    clinical review status
                    pending
                    content role
                    positive_indication_candidate
                    context span
                    end
                    1293
                    end exclusive
                    true
                    exact text
                    ment with ZOLADEX and flutamide should start 8 weeks prior to initiating radiation therapy and continue during radiation therapy [see Dosage and Administration ( 2.1 ) and Clinical Studies ( 14.1 )]. 1.2 Prostatic Carcinoma ZOLADEX is indicated in the palliative treatment of advanced carcinoma of the prostate [see Dosage and Administration ( 2.2 ) and Clinical Studies ( 14.2 )]. 1.3 Endometriosis ZOLADEX is indicated for the management of endometriosis, including pain relief and reduction of endometriotic lesions for the duration of therapy. Experience with ZOLADEX for the m
                    label id
                    c48edbf8-425f-4e11-8892-467e868d9fba
                    offset unit
                    unicode_code_points
                    source array index
                    0
                    source field
                    indications_and_usage_exact
                    source text sha256
                    f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                    start
                    712
                    current approval status
                    not_reconciled
                    duplicate text group
                    dup-0b8109182e4ee56caf59
                    extraction review status
                    automated_candidate_pending_source_review
                    generic names
                    1. GOSERELIN
                    id
                    ind-span-f0732bfe8d5c129a470a
                    label id
                    c48edbf8-425f-4e11-8892-467e868d9fba
                    positive predicate support span
                    end
                    956
                    end exclusive
                    true
                    exact text
                    is indicated
                    label id
                    c48edbf8-425f-4e11-8892-467e868d9fba
                    offset unit
                    unicode_code_points
                    source array index
                    0
                    source field
                    indications_and_usage_exact
                    source text sha256
                    f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                    start
                    944
                    qualifier mentions
                    1. context exact
                      rcinoma ZOLADEX is indicated in the palliative treatment of advanced carcinoma of the prostate [see Dosage and Administration ( 2.2 ) and Clinical Studies ( 14.2 )
                      kind
                      stage_or_setting
                      polarity
                      not_inferred
                      span
                      end
                      1031
                      end exclusive
                      true
                      exact text
                      advanced carcinoma of the prostate [see Dos
                      label id
                      c48edbf8-425f-4e11-8892-467e868d9fba
                      offset unit
                      unicode_code_points
                      source array index
                      0
                      source field
                      indications_and_usage_exact
                      source text sha256
                      f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                      start
                      988
                    regulatory links
                      schema version
                      0.1.0
                      source batch sha256
                      a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                      source defined aliases
                        source span
                        end
                        1093
                        end exclusive
                        true
                        exact text
                        1.2 Prostatic Carcinoma ZOLADEX is indicated in the palliative treatment of advanced carcinoma of the prostate [see Dosage and Administration ( 2.2 ) and Clinical Studies ( 14.2 )].
                        label id
                        c48edbf8-425f-4e11-8892-467e868d9fba
                        offset unit
                        unicode_code_points
                        source array index
                        0
                        source field
                        indications_and_usage_exact
                        source text sha256
                        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                        start
                        912
                        source url
                        https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                        spl effective date
                        2026-03-24
                        spl set id
                        294b168b-6e5f-4db9-bf70-d599271458b3
                        spl version
                        9
                        structured fields status
                        not_extracted_no_values_inferred_from_mentions
                        structured indication
                        age
                        Source null
                        approval pathway
                        Source null
                        biomarker and test
                        Source null
                        disease stage
                        Source null
                        limitations
                        Source null
                        line
                        Source null
                        prior therapy
                        Source null
                        regimen
                        Source null
                        tumor histology
                        Source null
                        use intent
                        tumor_directed_candidate
                        Passage 5 · positive indication candidate
                        application numbers
                        1. NDA019726
                        brand names
                        1. ZOLADEX
                        classification reasons
                        1. explicit_positive_indication_predicate
                        2. no_tumor_directed_keyword_in_positive_statement
                        clinical review status
                        pending
                        content role
                        positive_indication_candidate
                        context span
                        end
                        1459
                        end exclusive
                        true
                        exact text
                        tudies ( 14.1 )]. 1.2 Prostatic Carcinoma ZOLADEX is indicated in the palliative treatment of advanced carcinoma of the prostate [see Dosage and Administration ( 2.2 ) and Clinical Studies ( 14.2 )]. 1.3 Endometriosis ZOLADEX is indicated for the management of endometriosis, including pain relief and reduction of endometriotic lesions for the duration of therapy. Experience with ZOLADEX for the management of endometriosis has been limited to women 18 years of age and older treated for 6 months [see Dosage and Administration ( 2.3 ) and Clinical Studies ( 14.3
                        label id
                        c48edbf8-425f-4e11-8892-467e868d9fba
                        offset unit
                        unicode_code_points
                        source array index
                        0
                        source field
                        indications_and_usage_exact
                        source text sha256
                        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                        start
                        894
                        current approval status
                        not_reconciled
                        duplicate text group
                        dup-bff14a857ef9290077dd
                        extraction review status
                        automated_candidate_pending_source_review
                        generic names
                        1. GOSERELIN
                        id
                        ind-span-f2e4ebc17e6e8dc03a41
                        label id
                        c48edbf8-425f-4e11-8892-467e868d9fba
                        positive predicate support span
                        end
                        1132
                        end exclusive
                        true
                        exact text
                        is indicated
                        label id
                        c48edbf8-425f-4e11-8892-467e868d9fba
                        offset unit
                        unicode_code_points
                        source array index
                        0
                        source field
                        indications_and_usage_exact
                        source text sha256
                        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                        start
                        1120
                        qualifier mentions
                          regulatory links
                            schema version
                            0.1.0
                            source batch sha256
                            a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                            source defined aliases
                              source span
                              end
                              1259
                              end exclusive
                              true
                              exact text
                              1.3 Endometriosis ZOLADEX is indicated for the management of endometriosis, including pain relief and reduction of endometriotic lesions for the duration of therapy.
                              label id
                              c48edbf8-425f-4e11-8892-467e868d9fba
                              offset unit
                              unicode_code_points
                              source array index
                              0
                              source field
                              indications_and_usage_exact
                              source text sha256
                              f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                              start
                              1094
                              source url
                              https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                              spl effective date
                              2026-03-24
                              spl set id
                              294b168b-6e5f-4db9-bf70-d599271458b3
                              spl version
                              9
                              structured fields status
                              not_extracted_no_values_inferred_from_mentions
                              structured indication
                              age
                              Source null
                              approval pathway
                              Source null
                              biomarker and test
                              Source null
                              disease stage
                              Source null
                              limitations
                              Source null
                              line
                              Source null
                              prior therapy
                              Source null
                              regimen
                              Source null
                              tumor histology
                              Source null
                              use intent
                              non_oncology_or_unclear_candidate
                              Passage 6 · unclassified context
                              application numbers
                              1. NDA019726
                              brand names
                              1. ZOLADEX
                              classification reasons
                              1. no_unambiguous_positive_indication_predicate
                              clinical review status
                              pending
                              content role
                              unclassified_context
                              context span
                              end
                              1663
                              end exclusive
                              true
                              exact text
                              ) and Clinical Studies ( 14.2 )]. 1.3 Endometriosis ZOLADEX is indicated for the management of endometriosis, including pain relief and reduction of endometriotic lesions for the duration of therapy. Experience with ZOLADEX for the management of endometriosis has been limited to women 18 years of age and older treated for 6 months [see Dosage and Administration ( 2.3 ) and Clinical Studies ( 14.3 )]. 1.4 Endometrial Thinning ZOLADEX is indicated for use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding [see Dosage and Administration ( 2.4 ) and Clin
                              label id
                              c48edbf8-425f-4e11-8892-467e868d9fba
                              offset unit
                              unicode_code_points
                              source array index
                              0
                              source field
                              indications_and_usage_exact
                              source text sha256
                              f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                              start
                              1060
                              current approval status
                              not_reconciled
                              duplicate text group
                              dup-20035cbc4fae03c1610c
                              extraction review status
                              automated_candidate_pending_source_review
                              generic names
                              1. GOSERELIN
                              id
                              ind-span-9bec2217a415d5860a6a
                              label id
                              c48edbf8-425f-4e11-8892-467e868d9fba
                              positive predicate support span
                              Source null
                              qualifier mentions
                              1. context exact
                                r the management of endometriosis has been limited to women 18 years of age and older treated for 6 months [see Dosage and Administrati
                                kind
                                age
                                polarity
                                not_inferred
                                span
                                end
                                1361
                                end exclusive
                                true
                                exact text
                                18 years of age
                                label id
                                c48edbf8-425f-4e11-8892-467e868d9fba
                                offset unit
                                unicode_code_points
                                source array index
                                0
                                source field
                                indications_and_usage_exact
                                source text sha256
                                f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                start
                                1346
                              regulatory links
                                schema version
                                0.1.0
                                source batch sha256
                                a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                                source defined aliases
                                  source span
                                  end
                                  1463
                                  end exclusive
                                  true
                                  exact text
                                  Experience with ZOLADEX for the management of endometriosis has been limited to women 18 years of age and older treated for 6 months [see Dosage and Administration ( 2.3 ) and Clinical Studies ( 14.3 )].
                                  label id
                                  c48edbf8-425f-4e11-8892-467e868d9fba
                                  offset unit
                                  unicode_code_points
                                  source array index
                                  0
                                  source field
                                  indications_and_usage_exact
                                  source text sha256
                                  f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                  start
                                  1260
                                  source url
                                  https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                                  spl effective date
                                  2026-03-24
                                  spl set id
                                  294b168b-6e5f-4db9-bf70-d599271458b3
                                  spl version
                                  9
                                  structured fields status
                                  not_extracted_no_values_inferred_from_mentions
                                  structured indication
                                  age
                                  Source null
                                  approval pathway
                                  Source null
                                  biomarker and test
                                  Source null
                                  disease stage
                                  Source null
                                  limitations
                                  Source null
                                  line
                                  Source null
                                  prior therapy
                                  Source null
                                  regimen
                                  Source null
                                  tumor histology
                                  Source null
                                  use intent
                                  unclear
                                  Passage 7 · positive indication candidate
                                  application numbers
                                  1. NDA019726
                                  brand names
                                  1. ZOLADEX
                                  classification reasons
                                  1. explicit_positive_indication_predicate
                                  2. no_tumor_directed_keyword_in_positive_statement
                                  clinical review status
                                  pending
                                  content role
                                  positive_indication_candidate
                                  context span
                                  end
                                  1886
                                  end exclusive
                                  true
                                  exact text
                                  rience with ZOLADEX for the management of endometriosis has been limited to women 18 years of age and older treated for 6 months [see Dosage and Administration ( 2.3 ) and Clinical Studies ( 14.3 )]. 1.4 Endometrial Thinning ZOLADEX is indicated for use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding [see Dosage and Administration ( 2.4 ) and Clinical Studies ( 14.4 )]. 1.5 Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women. The estrogen and progesterone receptor values may help
                                  label id
                                  c48edbf8-425f-4e11-8892-467e868d9fba
                                  offset unit
                                  unicode_code_points
                                  source array index
                                  0
                                  source field
                                  indications_and_usage_exact
                                  source text sha256
                                  f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                  start
                                  1264
                                  current approval status
                                  not_reconciled
                                  duplicate text group
                                  dup-198674d8a01d1cdf68ae
                                  extraction review status
                                  automated_candidate_pending_source_review
                                  generic names
                                  1. GOSERELIN
                                  id
                                  ind-span-01bccafb253072426199
                                  label id
                                  c48edbf8-425f-4e11-8892-467e868d9fba
                                  positive predicate support span
                                  end
                                  1509
                                  end exclusive
                                  true
                                  exact text
                                  is indicated
                                  label id
                                  c48edbf8-425f-4e11-8892-467e868d9fba
                                  offset unit
                                  unicode_code_points
                                  source array index
                                  0
                                  source field
                                  indications_and_usage_exact
                                  source text sha256
                                  f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                  start
                                  1497
                                  qualifier mentions
                                    regulatory links
                                      schema version
                                      0.1.0
                                      source batch sha256
                                      a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                                      source defined aliases
                                        source span
                                        end
                                        1686
                                        end exclusive
                                        true
                                        exact text
                                        1.4 Endometrial Thinning ZOLADEX is indicated for use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding [see Dosage and Administration ( 2.4 ) and Clinical Studies ( 14.4 )].
                                        label id
                                        c48edbf8-425f-4e11-8892-467e868d9fba
                                        offset unit
                                        unicode_code_points
                                        source array index
                                        0
                                        source field
                                        indications_and_usage_exact
                                        source text sha256
                                        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                        start
                                        1464
                                        source url
                                        https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                                        spl effective date
                                        2026-03-24
                                        spl set id
                                        294b168b-6e5f-4db9-bf70-d599271458b3
                                        spl version
                                        9
                                        structured fields status
                                        not_extracted_no_values_inferred_from_mentions
                                        structured indication
                                        age
                                        Source null
                                        approval pathway
                                        Source null
                                        biomarker and test
                                        Source null
                                        disease stage
                                        Source null
                                        limitations
                                        Source null
                                        line
                                        Source null
                                        prior therapy
                                        Source null
                                        regimen
                                        Source null
                                        tumor histology
                                        Source null
                                        use intent
                                        non_oncology_or_unclear_candidate
                                        Passage 8 · positive indication candidate
                                        application numbers
                                        1. NDA019726
                                        brand names
                                        1. ZOLADEX
                                        classification reasons
                                        1. explicit_positive_indication_predicate
                                        2. tumor_or_malignant_hematology_words_in_positive_statement
                                        clinical review status
                                        pending
                                        content role
                                        positive_indication_candidate
                                        context span
                                        end
                                        2030
                                        end exclusive
                                        true
                                        exact text
                                        g ZOLADEX is indicated for use as an endometrial-thinning agent prior to endometrial ablation for dysfunctional uterine bleeding [see Dosage and Administration ( 2.4 ) and Clinical Studies ( 14.4 )]. 1.5 Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women. The estrogen and progesterone receptor values may help to predict whether ZOLADEX therapy is likely to be beneficial [see Dosage and Administration ( 2.5 ), Clinical Pharmacology ( 12.1 ), and Clinic
                                        label id
                                        c48edbf8-425f-4e11-8892-467e868d9fba
                                        offset unit
                                        unicode_code_points
                                        source array index
                                        0
                                        source field
                                        indications_and_usage_exact
                                        source text sha256
                                        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                        start
                                        1487
                                        current approval status
                                        not_reconciled
                                        duplicate text group
                                        dup-0f0d87ee2b7b3cb21074
                                        extraction review status
                                        automated_candidate_pending_source_review
                                        generic names
                                        1. GOSERELIN
                                        id
                                        ind-span-2c61d4f528406711b360
                                        label id
                                        c48edbf8-425f-4e11-8892-467e868d9fba
                                        positive predicate support span
                                        end
                                        1734
                                        end exclusive
                                        true
                                        exact text
                                        is indicated
                                        label id
                                        c48edbf8-425f-4e11-8892-467e868d9fba
                                        offset unit
                                        unicode_code_points
                                        source array index
                                        0
                                        source field
                                        indications_and_usage_exact
                                        source text sha256
                                        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                        start
                                        1722
                                        qualifier mentions
                                        1. context exact
                                          1.5 Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast canc
                                          kind
                                          stage_or_setting
                                          polarity
                                          not_inferred
                                          span
                                          end
                                          1734
                                          end exclusive
                                          true
                                          exact text
                                          Advanced Breast Cancer ZOLADEX is indicated
                                          label id
                                          c48edbf8-425f-4e11-8892-467e868d9fba
                                          offset unit
                                          unicode_code_points
                                          source array index
                                          0
                                          source field
                                          indications_and_usage_exact
                                          source text sha256
                                          f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                          start
                                          1691
                                        2. context exact
                                          ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women.
                                          kind
                                          stage_or_setting
                                          polarity
                                          not_inferred
                                          span
                                          end
                                          1817
                                          end exclusive
                                          true
                                          exact text
                                          advanced breast cancer in pre- and perimeno
                                          label id
                                          c48edbf8-425f-4e11-8892-467e868d9fba
                                          offset unit
                                          unicode_code_points
                                          source array index
                                          0
                                          source field
                                          indications_and_usage_exact
                                          source text sha256
                                          f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                          start
                                          1774
                                        regulatory links
                                          schema version
                                          0.1.0
                                          source batch sha256
                                          a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                                          source defined aliases
                                            source span
                                            end
                                            1830
                                            end exclusive
                                            true
                                            exact text
                                            1.5 Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women.
                                            label id
                                            c48edbf8-425f-4e11-8892-467e868d9fba
                                            offset unit
                                            unicode_code_points
                                            source array index
                                            0
                                            source field
                                            indications_and_usage_exact
                                            source text sha256
                                            f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                            start
                                            1687
                                            source url
                                            https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                                            spl effective date
                                            2026-03-24
                                            spl set id
                                            294b168b-6e5f-4db9-bf70-d599271458b3
                                            spl version
                                            9
                                            structured fields status
                                            not_extracted_no_values_inferred_from_mentions
                                            structured indication
                                            age
                                            Source null
                                            approval pathway
                                            Source null
                                            biomarker and test
                                            Source null
                                            disease stage
                                            Source null
                                            limitations
                                            Source null
                                            line
                                            Source null
                                            prior therapy
                                            Source null
                                            regimen
                                            Source null
                                            tumor histology
                                            Source null
                                            use intent
                                            tumor_directed_candidate
                                            Passage 9 · unclassified context
                                            application numbers
                                            1. NDA019726
                                            brand names
                                            1. ZOLADEX
                                            classification reasons
                                            1. no_unambiguous_positive_indication_predicate
                                            clinical review status
                                            pending
                                            content role
                                            unclassified_context
                                            context span
                                            end
                                            2141
                                            end exclusive
                                            true
                                            exact text
                                            Administration ( 2.4 ) and Clinical Studies ( 14.4 )]. 1.5 Advanced Breast Cancer ZOLADEX is indicated for use in the palliative treatment of advanced breast cancer in pre- and perimenopausal women. The estrogen and progesterone receptor values may help to predict whether ZOLADEX therapy is likely to be beneficial [see Dosage and Administration ( 2.5 ), Clinical Pharmacology ( 12.1 ), and Clinical Studies ( 14.5 )]. The automatic safety feature of the syringe aids in the prevention of needlestick injury.
                                            label id
                                            c48edbf8-425f-4e11-8892-467e868d9fba
                                            offset unit
                                            unicode_code_points
                                            source array index
                                            0
                                            source field
                                            indications_and_usage_exact
                                            source text sha256
                                            f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                            start
                                            1631
                                            current approval status
                                            not_reconciled
                                            duplicate text group
                                            dup-e5197c742d303bb84990
                                            extraction review status
                                            automated_candidate_pending_source_review
                                            generic names
                                            1. GOSERELIN
                                            id
                                            ind-span-e79756a6acdcbe6f06a0
                                            label id
                                            c48edbf8-425f-4e11-8892-467e868d9fba
                                            positive predicate support span
                                            Source null
                                            qualifier mentions
                                              regulatory links
                                                schema version
                                                0.1.0
                                                source batch sha256
                                                a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                                                source defined aliases
                                                  source span
                                                  end
                                                  2051
                                                  end exclusive
                                                  true
                                                  exact text
                                                  The estrogen and progesterone receptor values may help to predict whether ZOLADEX therapy is likely to be beneficial [see Dosage and Administration ( 2.5 ), Clinical Pharmacology ( 12.1 ), and Clinical Studies ( 14.5 )].
                                                  label id
                                                  c48edbf8-425f-4e11-8892-467e868d9fba
                                                  offset unit
                                                  unicode_code_points
                                                  source array index
                                                  0
                                                  source field
                                                  indications_and_usage_exact
                                                  source text sha256
                                                  f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                                  start
                                                  1831
                                                  source url
                                                  https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                                                  spl effective date
                                                  2026-03-24
                                                  spl set id
                                                  294b168b-6e5f-4db9-bf70-d599271458b3
                                                  spl version
                                                  9
                                                  structured fields status
                                                  not_extracted_no_values_inferred_from_mentions
                                                  structured indication
                                                  age
                                                  Source null
                                                  approval pathway
                                                  Source null
                                                  biomarker and test
                                                  Source null
                                                  disease stage
                                                  Source null
                                                  limitations
                                                  Source null
                                                  line
                                                  Source null
                                                  prior therapy
                                                  Source null
                                                  regimen
                                                  Source null
                                                  tumor histology
                                                  Source null
                                                  use intent
                                                  unclear
                                                  Passage 10 · unclassified context
                                                  application numbers
                                                  1. NDA019726
                                                  brand names
                                                  1. ZOLADEX
                                                  classification reasons
                                                  1. no_unambiguous_positive_indication_predicate
                                                  clinical review status
                                                  pending
                                                  content role
                                                  unclassified_context
                                                  context span
                                                  end
                                                  2141
                                                  end exclusive
                                                  true
                                                  exact text
                                                  esterone receptor values may help to predict whether ZOLADEX therapy is likely to be beneficial [see Dosage and Administration ( 2.5 ), Clinical Pharmacology ( 12.1 ), and Clinical Studies ( 14.5 )]. The automatic safety feature of the syringe aids in the prevention of needlestick injury.
                                                  label id
                                                  c48edbf8-425f-4e11-8892-467e868d9fba
                                                  offset unit
                                                  unicode_code_points
                                                  source array index
                                                  0
                                                  source field
                                                  indications_and_usage_exact
                                                  source text sha256
                                                  f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                                  start
                                                  1852
                                                  current approval status
                                                  not_reconciled
                                                  duplicate text group
                                                  dup-4f720cbd3389e054c890
                                                  extraction review status
                                                  automated_candidate_pending_source_review
                                                  generic names
                                                  1. GOSERELIN
                                                  id
                                                  ind-span-3a0ea744c09594bc2642
                                                  label id
                                                  c48edbf8-425f-4e11-8892-467e868d9fba
                                                  positive predicate support span
                                                  Source null
                                                  qualifier mentions
                                                    regulatory links
                                                      schema version
                                                      0.1.0
                                                      source batch sha256
                                                      a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
                                                      source defined aliases
                                                        source span
                                                        end
                                                        2141
                                                        end exclusive
                                                        true
                                                        exact text
                                                        The automatic safety feature of the syringe aids in the prevention of needlestick injury.
                                                        label id
                                                        c48edbf8-425f-4e11-8892-467e868d9fba
                                                        offset unit
                                                        unicode_code_points
                                                        source array index
                                                        0
                                                        source field
                                                        indications_and_usage_exact
                                                        source text sha256
                                                        f3006870e5ef0e2cb7ab08b9f447ab89489aaf269ca308b05d54a319621aab68
                                                        start
                                                        2052
                                                        source url
                                                        https://api.fda.gov/drug/label.json?search=id%3A%22c48edbf8-425f-4e11-8892-467e868d9fba%22
                                                        spl effective date
                                                        2026-03-24
                                                        spl set id
                                                        294b168b-6e5f-4db9-bf70-d599271458b3
                                                        spl version
                                                        9
                                                        structured fields status
                                                        not_extracted_no_values_inferred_from_mentions
                                                        structured indication
                                                        age
                                                        Source null
                                                        approval pathway
                                                        Source null
                                                        biomarker and test
                                                        Source null
                                                        disease stage
                                                        Source null
                                                        limitations
                                                        Source null
                                                        line
                                                        Source null
                                                        prior therapy
                                                        Source null
                                                        regimen
                                                        Source null
                                                        tumor histology
                                                        Source null
                                                        use intent
                                                        unclear

                                                        Preserved source evidence · Not medical advice