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Heparin Sodium

NDC 63323-519 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212441
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsHEPARIN SODIUM (200 [USP'U]/100mL)
Marketing started20200724
Package count2

External sources

Source: openFDA. Public-domain (CC0).