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LABELS · af340f13-7954-4974-845d-ae55e0b56512

Fragmin

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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
2025-09-30
Captured
2026-09-09T23:37:58.719708+00:00
Current indication reconciliation
Not reconciled
Boxed warning in this label
  1. WARNING: SPINAL/EPIDURAL HEMATOMAS Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. Factors that can increase the risk of developing epidural or spinal hematomas in these patients include: • Use of indwelling epidural catheters • Concomitant use of other drugs that affect hemostasis, such as non-steroidal anti-inflammatory drugs (NSAIDs), platelet inhibitors, other anticoagulants. • A history of traumatic or repeated epidural or spinal punctures • A history of spinal deformity or spinal surgery • Optimal timing between the administration of FRAGMIN and neuraxial procedures is not known Monitor patients frequently for signs and symptoms of neurological impairment. If neurological compromise is noted, urgent treatment is necessary. Consider the benefits and risks before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis [see Warnings and Precautions (5.1) and Drug Interactions (7) ] . WARNING: SPINAL/EPIDURAL HEMATOMAS See full prescribing information for complete boxed warning. Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. Factors that can increase the risk of developing epidural or spinal hematomas in these patients include: • Use of indwelling epidural catheters • Concomitant use of other drugs that affect hemostasis, such as non-steroidal anti-inflammatory drugs (NSAIDs), platelet inhibitors, other anticoagulants. • A history of traumatic or repeated epidural or spinal punctures • A history of spinal deformity or spinal surgery • Optimal timing between the administration of FRAGMIN and neuraxial procedures is not known Monitor patients frequently for signs and symptoms of neurological impairment. If neurological compromise is noted, urgent treatment is necessary. Consider the benefits and risks before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis ( 5.1 , 7 ).

Indications and usage: exact source text

  1. 1 INDICATIONS AND USAGE FRAGMIN is a low molecular weight heparin (LMWH) indicated for • Prophylaxis of ischemic complications of unstable angina and non-Q-wave myocardial infarction ( 1.1 ) • Prophylaxis of deep vein thrombosis (DVT) in abdominal surgery, hip replacement surgery or medical patients with severely restricted mobility during acute illness ( 1.2 ) • Extended treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence in adult patients with cancer. In these patients, the FRAGMIN therapy begins with the initial VTE treatment and continues for six months ( 1.3 ) • Treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence in pediatric patients from birth (gestational age at least 35 weeks) ( 1.4 ) • Limitations of Use FRAGMIN is not indicated for the acute treatment of VTE ( 1.5 ) 1.1 Prophylaxis of Ischemic Complications in Unstable Angina and Non-Q-Wave Myocardial Infarction FRAGMIN Injection is indicated for the prophylaxis of ischemic complications in unstable angina and non-Q-wave myocardial infarction, when concurrently administered with aspirin therapy [see Clinical Studies (14.1) ] . 1.2 Prophylaxis of Deep Vein Thrombosis FRAGMIN is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE): • In patients undergoing hip replacement surgery [see Clinical Studies (14.2) ] ; • In patients undergoing abdominal surgery who are at risk for thromboembolic complications [see Clinical Studies (14.3) ] ; • In medical patients who are at risk for thromboembolic complications due to severely restricted mobility during acute illness [see Clinical Studies (14.4) ] . 1.3 Extended Treatment of Symptomatic Venous Thromboembolism (VTE) in Adult Patients with Cancer FRAGMIN is indicated for the extended treatment of symptomatic venous thromboembolism (VTE) (proximal DVT and/or PE), to reduce the recurrence of VTE in adult patients with cancer. In these patients, the FRAGMIN therapy begins with the initial VTE treatment and continues for six months [see Clinical Studies (14.5) ] . 1.4 Treatment of Symptomatic Venous Thromboembolism (VTE) in Pediatric Patients FRAGMIN is indicated for the treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence of VTE in pediatric patients from birth (gestational age at least 35 weeks) . 1.5 Limitations of Use FRAGMIN is not indicated for the acute treatment of VTE.
Full extracted label fields
application numbers
  1. NDA020287
boxed warning exact
  1. WARNING: SPINAL/EPIDURAL HEMATOMAS Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. Factors that can increase the risk of developing epidural or spinal hematomas in these patients include: • Use of indwelling epidural catheters • Concomitant use of other drugs that affect hemostasis, such as non-steroidal anti-inflammatory drugs (NSAIDs), platelet inhibitors, other anticoagulants. • A history of traumatic or repeated epidural or spinal punctures • A history of spinal deformity or spinal surgery • Optimal timing between the administration of FRAGMIN and neuraxial procedures is not known Monitor patients frequently for signs and symptoms of neurological impairment. If neurological compromise is noted, urgent treatment is necessary. Consider the benefits and risks before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis [see Warnings and Precautions (5.1) and Drug Interactions (7) ] . WARNING: SPINAL/EPIDURAL HEMATOMAS See full prescribing information for complete boxed warning. Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. Factors that can increase the risk of developing epidural or spinal hematomas in these patients include: • Use of indwelling epidural catheters • Concomitant use of other drugs that affect hemostasis, such as non-steroidal anti-inflammatory drugs (NSAIDs), platelet inhibitors, other anticoagulants. • A history of traumatic or repeated epidural or spinal punctures • A history of spinal deformity or spinal surgery • Optimal timing between the administration of FRAGMIN and neuraxial procedures is not known Monitor patients frequently for signs and symptoms of neurological impairment. If neurological compromise is noted, urgent treatment is necessary. Consider the benefits and risks before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis ( 5.1 , 7 ).
brand names
  1. Fragmin
current indication status
not_reconciled
dailymed set url
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=23527b8b-9b28-4e6d-9751-33b143975ac7
generic names
  1. DALTEPARIN SODIUM
id
af340f13-7954-4974-845d-ae55e0b56512
indications and usage exact
  1. 1 INDICATIONS AND USAGE FRAGMIN is a low molecular weight heparin (LMWH) indicated for • Prophylaxis of ischemic complications of unstable angina and non-Q-wave myocardial infarction ( 1.1 ) • Prophylaxis of deep vein thrombosis (DVT) in abdominal surgery, hip replacement surgery or medical patients with severely restricted mobility during acute illness ( 1.2 ) • Extended treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence in adult patients with cancer. In these patients, the FRAGMIN therapy begins with the initial VTE treatment and continues for six months ( 1.3 ) • Treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence in pediatric patients from birth (gestational age at least 35 weeks) ( 1.4 ) • Limitations of Use FRAGMIN is not indicated for the acute treatment of VTE ( 1.5 ) 1.1 Prophylaxis of Ischemic Complications in Unstable Angina and Non-Q-Wave Myocardial Infarction FRAGMIN Injection is indicated for the prophylaxis of ischemic complications in unstable angina and non-Q-wave myocardial infarction, when concurrently administered with aspirin therapy [see Clinical Studies (14.1) ] . 1.2 Prophylaxis of Deep Vein Thrombosis FRAGMIN is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE): • In patients undergoing hip replacement surgery [see Clinical Studies (14.2) ] ; • In patients undergoing abdominal surgery who are at risk for thromboembolic complications [see Clinical Studies (14.3) ] ; • In medical patients who are at risk for thromboembolic complications due to severely restricted mobility during acute illness [see Clinical Studies (14.4) ] . 1.3 Extended Treatment of Symptomatic Venous Thromboembolism (VTE) in Adult Patients with Cancer FRAGMIN is indicated for the extended treatment of symptomatic venous thromboembolism (VTE) (proximal DVT and/or PE), to reduce the recurrence of VTE in adult patients with cancer. In these patients, the FRAGMIN therapy begins with the initial VTE treatment and continues for six months [see Clinical Studies (14.5) ] . 1.4 Treatment of Symptomatic Venous Thromboembolism (VTE) in Pediatric Patients FRAGMIN is indicated for the treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence of VTE in pediatric patients from birth (gestational age at least 35 weeks) . 1.5 Limitations of Use FRAGMIN is not indicated for the acute treatment of VTE.
indications and usage tables exact
    is original packager
    1. true
    manufacturer names
    1. Pfizer Laboratories Div Pfizer Inc
    matched search terms
    1. cancer
    package ndcs
    1. 0069-0195-01
    2. 0069-0195-02
    3. 0069-0196-01
    4. 0069-0196-02
    5. 0069-0206-01
    6. 0069-0206-02
    7. 0069-0217-01
    8. 0069-0217-02
    9. 0069-0220-01
    10. 0069-0220-02
    11. 0069-0223-01
    12. 0069-0223-02
    product ndcs
    1. 0069-0195
    2. 0069-0196
    3. 0069-0206
    4. 0069-0217
    5. 0069-0220
    6. 0069-0223
    7. 0069-0228
    8. 0069-0232
    9. 0069-0253
    product types
    1. HUMAN PRESCRIPTION DRUG
    recent major changes exact
    1. Indications and Usage, Treatment of Symptomatic Venous Thromboembolism (VTE) in Pediatric Patients ( 1.4 ) 10/2024 Dosage and Administration, Treatment of Symptomatic Venous Thromboembolism (VTE) in Pediatric Patients ( 2.4 ) 10/2024 Dosage and Administration, Dose Reductions for Thrombocytopenia in Adult Patients with Cancer and in Pediatric Patients with Symptomatic VTE ( 2.5 ) 10/2024
    record type
    complete_spl_indications_section_candidate
    routes
    1. SUBCUTANEOUS
    rxcuis
    1. 978725
    2. 978727
    3. 978733
    4. 978735
    5. 978736
    6. 978737
    7. 978740
    8. 978741
    9. 978744
    10. 978745
    11. 978746
    12. 978747
    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%22af340f13-7954-4974-845d-ae55e0b56512%22
    spl effective date
    2025-09-30
    spl effective time
    20250930
    spl set id
    23527b8b-9b28-4e6d-9751-33b143975ac7
    spl version
    27
    substance names
    1. DALTEPARIN SODIUM
    uniis
    1. 12M44VTJ7B
    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
    Drugs@FDA application source records
    1. application number
      NDA020287
      payload
      all indexed label documents
      1. Appl No
        020287
        Application Docs Date
        2015-01-30 00:00:00
        Application Docs ID
        12420
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        62
        Submission Type
        SUPPL
      2. Appl No
        020287
        Application Docs Date
        1999-03-30 00:00:00
        Application Docs ID
        34473
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        8
        Submission Type
        SUPPL
      3. Appl No
        020287
        Application Docs Date
        1999-05-25 00:00:00
        Application Docs ID
        34474
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        10
        Submission Type
        SUPPL
      4. Appl No
        020287
        Application Docs Date
        2000-08-03 00:00:00
        Application Docs ID
        34475
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        18
        Submission Type
        SUPPL
      5. Appl No
        020287
        Application Docs Date
        2003-12-16 00:00:00
        Application Docs ID
        34476
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        32
        Submission Type
        SUPPL
      6. Appl No
        020287
        Application Docs Date
        2007-05-07 00:00:00
        Application Docs ID
        34477
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        35
        Submission Type
        SUPPL
      7. Appl No
        020287
        Application Docs Date
        2009-12-30 00:00:00
        Application Docs ID
        34478
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        49
        Submission Type
        SUPPL
      8. Appl No
        020287
        Application Docs Date
        2010-10-25 00:00:00
        Application Docs ID
        34479
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        50
        Submission Type
        SUPPL
      9. Appl No
        020287
        Application Docs Date
        2015-10-07 00:00:00
        Application Docs ID
        34480
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        63
        Submission Type
        SUPPL
      10. Appl No
        020287
        Application Docs Date
        2016-08-04 00:00:00
        Application Docs ID
        44997
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        67
        Submission Type
        SUPPL
      11. Appl No
        020287
        Application Docs Date
        2017-05-12 00:00:00
        Application Docs ID
        48370
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        69
        Submission Type
        SUPPL
      12. Appl No
        020287
        Application Docs Date
        2019-05-16 00:00:00
        Application Docs ID
        58751
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        72
        Submission Type
        SUPPL
      all submission records
      1. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        81
        Submission Status
        AP
        Submission Status Date
        2024-10-24 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      2. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        2
        Submission No
        80
        Submission Status
        AP
        Submission Status Date
        2024-10-15 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      3. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        76
        Submission Status
        AP
        Submission Status Date
        2020-12-05 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      4. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        75
        Submission Status
        AP
        Submission Status Date
        2020-06-26 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      5. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        74
        Submission Status
        AP
        Submission Status Date
        2020-06-26 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      6. Appl No
        020287
        Review Priority
        PRIORITY
        Submission Class Code ID
        2
        Submission No
        72
        Submission Status
        AP
        Submission Status Date
        2019-05-16 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      7. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        69
        Submission Status
        AP
        Submission Status Date
        2017-05-12 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      8. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        4
        Submission No
        68
        Submission Status
        AP
        Submission Status Date
        2017-01-26 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      9. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        67
        Submission Status
        AP
        Submission Status Date
        2016-08-04 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      10. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        63
        Submission Status
        AP
        Submission Status Date
        2015-09-29 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      11. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        62
        Submission Status
        AP
        Submission Status Date
        2015-01-27 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      12. Appl No
        020287
        Review Priority
        STANDARD
        Submission Class Code ID
        4
        Submission No
        61
        Submission Status
        AP
        Submission Status Date
        2013-10-22 00:00:00
        Submission Type
        SUPPL
        Submissions Public Notes
      application number
      NDA020287
      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
      2024-10-24
      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
        020287
        Application Docs Date
        2024-12-02 00:00:00
        Application Docs ID
        79934
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        80
        Submission Type
        SUPPL
      official application record
      Appl No
      020287
      Appl Public Notes
      Appl Type
      NDA
      Sponsor Name
      PFIZER
      openfda application present
      true
      products
      1. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        001
        Reference Drug
        1
        Reference Standard
        0
        Strength
        2,500IU/0.2ML (12,500IU/ML)
        marketing status
        1. Prescription
      2. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        002
        Reference Drug
        0
        Reference Standard
        0
        Strength
        10,000IU/0.4ML (25,000IU/ML)
        marketing status
        1. Discontinued
      3. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        003
        Reference Drug
        1
        Reference Standard
        0
        Strength
        5,000IU/0.2ML (25,000IU/ML)
        marketing status
        1. Prescription
      4. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        004
        Reference Drug
        1
        Reference Standard
        0
        Strength
        10,000IU/ML (10,000IU/ML)
        marketing status
        1. Prescription
      5. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        005
        Reference Drug
        1
        Reference Standard
        0
        Strength
        7,500IU/0.3ML (25,000IU/ML)
        marketing status
        1. Prescription
      6. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        006
        Reference Drug
        1
        Reference Standard
        1
        Strength
        95,000IU/3.8ML (25,000IU/ML)
        marketing status
        1. Prescription
      7. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        007
        Reference Drug
        0
        Reference Standard
        0
        Strength
        95,000IU/9.5ML (10,000IU/ML)
        marketing status
        1. Discontinued
      8. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;INJECTION
        Product No
        008
        Reference Drug
        0
        Reference Standard
        0
        Strength
        7,500 IU/0.75ML
        marketing status
        1. Discontinued
      9. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        009
        Reference Drug
        1
        Reference Standard
        0
        Strength
        12,500IU/0.5ML (25,000IU/ML)
        marketing status
        1. Prescription
      10. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        010
        Reference Drug
        1
        Reference Standard
        0
        Strength
        15,000IU/0.6ML (25,000IU/ML)
        marketing status
        1. Prescription
      11. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        011
        Reference Drug
        1
        Reference Standard
        0
        Strength
        18,000IU/0.72ML (25,000IU/ML)
        marketing status
        1. Prescription
      12. Active Ingredient
        DALTEPARIN SODIUM
        Appl No
        020287
        Drug Name
        FRAGMIN
        Form
        INJECTABLE;SUBCUTANEOUS
        Product No
        012
        Reference Drug
        1
        Reference Standard
        0
        Strength
        10,000IU/4ML (2,500IU/ML)
        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. NDA020287
    brand names
    1. Fragmin
    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
    286
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                                                                            tients with Cancer FRAGMIN is indicated for the extended treatment of symptomatic venous thromboembolism (VTE) (proximal DVT and/or PE), to reduce the recurrence of VTE in adult patients with cancer. In these patients, the FRAGMIN therapy begins with the initial VTE treatment and continues for six months [see Clinical Studies (14.5) ] . 1.4 Treatment of Symptomatic Venous Thromboembolism (VTE) in Pediatric Patients FRAGMIN is indicated for the treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence of VTE in p
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                                                                                  In these patients, the FRAGMIN therapy begins with the initial VTE treatment and continues for six months [see Clinical Studies (14.5) ] .
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                                                                                  reduce the recurrence of VTE in adult patients with cancer. In these patients, the FRAGMIN therapy begins with the initial VTE treatment and continues for six months [see Clinical Studies (14.5) ] . 1.4 Treatment of Symptomatic Venous Thromboembolism (VTE) in Pediatric Patients FRAGMIN is indicated for the treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence of VTE in pediatric patients from birth (gestational age at least 35 weeks) . 1.5 Limitations of Use FRAGMIN is not indicated for the acute treatment of VTE.
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                                                                                      1.4 Treatment of Symptomatic Venous Thromboembolism (VTE) in Pediatric Patients FRAGMIN is indicated for the treatment of symptomatic venous thromboembolism (VTE) to reduce the recurrence of VTE in pediatric patients from birth (gestational age at least 35 weeks) .
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                                                                                            Preserved source evidence · Not medical advice