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
- 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 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
- NDA020287
- boxed warning exact
- 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
- 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
- DALTEPARIN SODIUM
- id
- af340f13-7954-4974-845d-ae55e0b56512
- indications and usage exact
- 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
- true
- manufacturer names
- Pfizer Laboratories Div Pfizer Inc
- matched search terms
- cancer
- package ndcs
- 0069-0195-01
- 0069-0195-02
- 0069-0196-01
- 0069-0196-02
- 0069-0206-01
- 0069-0206-02
- 0069-0217-01
- 0069-0217-02
- 0069-0220-01
- 0069-0220-02
- 0069-0223-01
- 0069-0223-02
- product ndcs
- 0069-0195
- 0069-0196
- 0069-0206
- 0069-0217
- 0069-0220
- 0069-0223
- 0069-0228
- 0069-0232
- 0069-0253
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- 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
- SUBCUTANEOUS
- rxcuis
- 978725
- 978727
- 978733
- 978735
- 978736
- 978737
- 978740
- 978741
- 978744
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- 978746
- 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
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- sha256
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- 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
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- spl version
- 27
- substance names
- DALTEPARIN SODIUM
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Drugs@FDA application source records
- application number
- NDA020287
- payload
- all indexed label documents
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2015/020287s062lbl.pdf
- Submission No
- 62
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/1999/20287s8lbl.pdf
- Submission No
- 8
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/nda/99/020287S10_Fragmin_prntlbl.pdf
- Submission No
- 10
- Submission Type
- SUPPL
- Appl No
- 020287
- Application Docs Date
- 2000-08-03 00:00:00
- Application Docs ID
- 34475
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- 0
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- 2
- Application Docs URL
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- Submission No
- 18
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2003/20287se1-032_fragmin_lbl.pdf
- Submission No
- 32
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2007/020287s035lbl.pdf
- Submission No
- 35
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020287s049lbl.pdf
- Submission No
- 49
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2010/020287s050lbl.pdf
- Submission No
- 50
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2015/020287s063lbl.pdf
- Submission No
- 63
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020287s067lbl.pdf
- Submission No
- 67
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2017/020287s069lbl.pdf
- Submission No
- 69
- Submission Type
- SUPPL
- 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
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2019/020287s072lbl.pdf
- Submission No
- 72
- Submission Type
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- 020287
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- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 81
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- Submission Status Date
- 2024-10-24 00:00:00
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- Appl No
- 020287
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- Submission Class Code ID
- 2
- Submission No
- 80
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- AP
- Submission Status Date
- 2024-10-15 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- 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
- 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
- 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
- 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
- Appl No
- 020287
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 69
- Submission Status
- AP
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- 2017-05-12 00:00:00
- Submission Type
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- Appl No
- 020287
- Review Priority
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- 4
- Submission No
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- 2017-01-26 00:00:00
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- Appl No
- 020287
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- Submission No
- 67
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- 2016-08-04 00:00:00
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- Submissions Public Notes
- Appl No
- 020287
- Review Priority
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- 3
- Submission No
- 63
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- Submission Status Date
- 2015-09-29 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 020287
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 62
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- AP
- Submission Status Date
- 2015-01-27 00:00:00
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- Appl No
- 020287
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- 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
- drugsfda url
- https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=020287
- 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
- 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
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/020287Orig1s080lbl.pdf
- 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
- 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
- Prescription
- 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
- Discontinued
- 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)
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- Active Ingredient
- DALTEPARIN SODIUM
- Appl No
- 020287
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- FRAGMIN
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- 004
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- 0
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- 10,000IU/ML (10,000IU/ML)
- marketing status
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- 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
- Prescription
- Active Ingredient
- DALTEPARIN SODIUM
- Appl No
- 020287
- Drug Name
- FRAGMIN
- Form
- INJECTABLE;SUBCUTANEOUS
- Product No
- 006
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- 1
- Reference Standard
- 1
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- 95,000IU/3.8ML (25,000IU/ML)
- marketing status
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- Active Ingredient
- DALTEPARIN SODIUM
- Appl No
- 020287
- Drug Name
- FRAGMIN
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- INJECTABLE;SUBCUTANEOUS
- Product No
- 007
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- 0
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- 0
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- 95,000IU/9.5ML (10,000IU/ML)
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- DALTEPARIN SODIUM
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- 020287
- Drug Name
- FRAGMIN
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- Product No
- 008
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- 0
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- 7,500 IU/0.75ML
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- Discontinued
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- DALTEPARIN SODIUM
- Appl No
- 020287
- Drug Name
- FRAGMIN
- Form
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- Strength
- 12,500IU/0.5ML (25,000IU/ML)
- marketing status
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- Active Ingredient
- DALTEPARIN SODIUM
- Appl No
- 020287
- Drug Name
- FRAGMIN
- Form
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- 010
- Reference Drug
- 1
- Reference Standard
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- Strength
- 15,000IU/0.6ML (25,000IU/ML)
- marketing status
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- Appl No
- 020287
- Drug Name
- FRAGMIN
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- Strength
- 18,000IU/0.72ML (25,000IU/ML)
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- Appl No
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- Drug Name
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- Reference Drug
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- Reference Standard
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- Strength
- 10,000IU/4ML (2,500IU/ML)
- marketing status
- Prescription
Source passages and status connections
Passage 1 · positive indication candidate
- application numbers
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- brand names
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- 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 me
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Passage 13 · positive indication candidate
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Passage 14 · unclassified context
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Passage 15 · positive indication candidate
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- tric 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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Preserved source evidence · Not medical advice
Triangle