LABELS · aacc35a2-0e82-4ba7-bec1-297802d4fa44
Aromasin
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
- 2025-12-24
- Captured
- 2026-09-09T23:37:54.830918+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- 1 INDICATIONS AND USAGE AROMASIN is an aromatase inhibitor indicated for: • adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14.1 ). • treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy ( 14.2 ). 1.1 Adjuvant Treatment of Postmenopausal Women AROMASIN is indicated for adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy [see Clinical Studies (14.1) ]. 1.2 Advanced Breast Cancer in Postmenopausal Women AROMASIN is indicated for the treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy [see Clinical Studies (14.2) ].
Full extracted label fields
- application numbers
- NDA020753
- boxed warning exact
- brand names
- Aromasin
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cf066b7a-032a-416c-8d40-15ba581423e3
- generic names
- EXEMESTANE
- id
- aacc35a2-0e82-4ba7-bec1-297802d4fa44
- indications and usage exact
- 1 INDICATIONS AND USAGE AROMASIN is an aromatase inhibitor indicated for: • adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14.1 ). • treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy ( 14.2 ). 1.1 Adjuvant Treatment of Postmenopausal Women AROMASIN is indicated for adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy [see Clinical Studies (14.1) ]. 1.2 Advanced Breast Cancer in Postmenopausal Women AROMASIN is indicated for the treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy [see Clinical Studies (14.2) ].
- indications and usage tables exact
- is original packager
- true
- manufacturer names
- Pharmacia & Upjohn Company LLC
- matched search terms
- cancer
- package ndcs
- 0009-7663-04
- product ndcs
- 0009-7663
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- record type
- complete_spl_indications_section_candidate
- routes
- ORAL
- rxcuis
- 261317
- 310261
- source batch
- file
- /private/tmp/cancer-full-research/indications/raw/labels-00500.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
- 500
- total
- 830
- sha256
- 424ccf5bc67db0a96ee2c35ed913dd5894642716182773d81ca19cdfb9ba32f3
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22aacc35a2-0e82-4ba7-bec1-297802d4fa44%22
- spl effective date
- 2025-12-24
- spl effective time
- 20251224
- spl set id
- cf066b7a-032a-416c-8d40-15ba581423e3
- spl version
- 24
- substance names
- EXEMESTANE
- uniis
- NY22HMQ4BX
- verification flags
- oncology_keyword_candidate_not_clinically_classified
- spl_text_not_verified_identical_to_latest_approved_label
- individual_indications_not_split_or_reconciled
Drugs@FDA application source records
- application number
- NDA020753
- payload
- all indexed label documents
- Appl No
- 020753
- Application Docs Date
- 1999-10-21 00:00:00
- Application Docs ID
- 13341
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/1999/20753LBL.PDF
- Submission No
- 1
- Submission Type
- ORIG
- Appl No
- 020753
- Application Docs Date
- 2003-12-02 00:00:00
- Application Docs ID
- 13342
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2003/20753slr003_aromasin_lbl.pdf
- Submission No
- 3
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2004-09-29 00:00:00
- Application Docs ID
- 13343
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2004/20753s005lbl.pdf
- Submission No
- 5
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2005-10-07 00:00:00
- Application Docs ID
- 13344
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2005/020753s006lbl.pdf
- Submission No
- 6
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2011-03-28 00:00:00
- Application Docs ID
- 13345
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020753s009s011s012lbl.pdf
- Submission No
- 9
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2011-03-28 00:00:00
- Application Docs ID
- 13346
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020753s009s011s012lbl.pdf
- Submission No
- 11
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2011-03-28 00:00:00
- Application Docs ID
- 13347
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020753s009s011s012lbl.pdf
- Submission No
- 12
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2013-02-20 00:00:00
- Application Docs ID
- 13348
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020753s014lbl.pdf
- Submission No
- 14
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2014-05-06 00:00:00
- Application Docs ID
- 13349
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020753s015s016lbl.pdf
- Submission No
- 16
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2016-07-27 00:00:00
- Application Docs ID
- 13350
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020753s018lbl.pdf
- Submission No
- 18
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2014-05-06 00:00:00
- Application Docs ID
- 35273
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020753s015s016lbl.pdf
- Submission No
- 15
- Submission Type
- SUPPL
- Appl No
- 020753
- Application Docs Date
- 2018-05-22 00:00:00
- Application Docs ID
- 54284
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2018/020753s020lbl.pdf
- Submission No
- 20
- Submission Type
- SUPPL
- all submission records
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 25
- Submission Status
- AP
- Submission Status Date
- 2024-12-16 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 22
- Submission Status
- AP
- Submission Status Date
- 2021-11-17 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 20
- Submission Status
- AP
- Submission Status Date
- 2018-05-18 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 18
- Submission Status
- AP
- Submission Status Date
- 2016-07-25 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 4
- Submission No
- 17
- Submission Status
- AP
- Submission Status Date
- 2014-07-28 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 16
- Submission Status
- AP
- Submission Status Date
- 2014-05-02 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 15
- Submission Status
- AP
- Submission Status Date
- 2014-05-02 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 14
- Submission Status
- AP
- Submission Status Date
- 2013-02-15 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- UNKNOWN
- Submission Class Code ID
- 3
- Submission No
- 12
- Submission Status
- AP
- Submission Status Date
- 2011-03-25 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 11
- Submission Status
- AP
- Submission Status Date
- 2011-03-25 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 9
- Submission Status
- AP
- Submission Status Date
- 2011-03-25 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020753
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 7
- Submission Status
- AP
- Submission Status Date
- 2008-12-24 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- application number
- NDA020753
- approval interpretation
- Application linkage and approved submission are not indication-level current approval verification
- current indication status
- not_reconciled
- drugsfda url
- https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=020753
- has approved submission record
- true
- latest approved submission date
- 2024-12-16
- 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
- Appl No
- 020753
- Application Docs Date
- 2024-12-17 00:00:00
- Application Docs ID
- 80601
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2024/020753s025lbl.pdf
- Submission No
- 25
- Submission Type
- SUPPL
- official application record
- Appl No
- 020753
- Appl Public Notes
- Appl Type
- NDA
- Sponsor Name
- PFIZER
- openfda application present
- true
- products
- Active Ingredient
- EXEMESTANE
- Appl No
- 020753
- Drug Name
- AROMASIN
- Form
- TABLET;ORAL
- Product No
- 001
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- 25MG
- marketing status
- Prescription
Source passages and status connections
Passage 1 · indication intro context
- application numbers
- NDA020753
- brand names
- Aromasin
- classification reasons
- explicit_positive_indication_predicate
- no_tumor_directed_keyword_in_positive_statement
- incomplete_colon_led_indication_intro
- clinical review status
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- content role
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- 273
- end exclusive
- true
- exact text
- 1 INDICATIONS AND USAGE AROMASIN is an aromatase inhibitor indicated for: • adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a tot
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- start
- 0
- current approval status
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- duplicate text group
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- extraction review status
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- generic names
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- 68
- end exclusive
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- is an aromatase inhibitor indicated
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- source field
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- start
- 33
- qualifier mentions
- regulatory links
- schema version
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- source batch sha256
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- source defined aliases
- source span
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- end exclusive
- true
- exact text
- 1 INDICATIONS AND USAGE AROMASIN is an aromatase inhibitor indicated for:
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- source text sha256
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- start
- 0
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22aacc35a2-0e82-4ba7-bec1-297802d4fa44%22
- spl effective date
- 2025-12-24
- spl set id
- cf066b7a-032a-416c-8d40-15ba581423e3
- spl version
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- 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
- not_applicable
Passage 2 · unclassified context
- application numbers
- NDA020753
- brand names
- Aromasin
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 540
- end exclusive
- true
- exact text
- 1 INDICATIONS AND USAGE AROMASIN is an aromatase inhibitor indicated for: • adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14.1 ). • treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy ( 14.2 ). 1.1 Adjuvant Treatment of Postmenopausal Women AROMASIN is indicated f
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- start
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- • adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have
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- start
- 76
- context exact
- ASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14.1 ).
- kind
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- not_inferred
- span
- end
- 335
- end exclusive
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- exact text
- adjuvant hormonal therapy ( 14
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- start
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- context exact
- l women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14.1 ).
- kind
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- exact text
- who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14
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- regulatory links
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- source defined aliases
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- • adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14.1 ).
- label id
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- offset unit
- unicode_code_points
- source array index
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- source field
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- source text sha256
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- start
- 74
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22aacc35a2-0e82-4ba7-bec1-297802d4fa44%22
- spl effective date
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- spl set id
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- spl version
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- structured fields status
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- Source null
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- 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 3 · unclassified context
- application numbers
- NDA020753
- brand names
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- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
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- content role
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- context span
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- end exclusive
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- exact text
- positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN for completion of a total of five consecutive years of adjuvant hormonal therapy ( 14.1 ). • treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy ( 14.2 ). 1.1 Adjuvant Treatment of Postmenopausal Women AROMASIN is indicated for adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three
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- • treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy ( 14.2 ).
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- start
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Preserved source evidence · Not medical advice
Triangle