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Heparin Sodium

NDC 71839-117 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerBE Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214804
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsHEPARIN SODIUM (2000 [USP'U]/2mL)
Marketing started20201229
Package count1

External sources

Source: openFDA. Public-domain (CC0).