# Heparin Sodium

NDC: 72603-214
Generic name: Heparin Sodium
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20240401

FDA application: ANDA211007

## Active ingredients

- HEPARIN SODIUM: 5000 [USP'U]/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-214"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-214
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c4fa6d34-e76b-4c3c-b74d-21ce41432a04