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Heparin Sodium

NDC 0781-3541 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSandoz Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203198
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsHEPARIN SODIUM (20000 [USP'U]/mL)
Marketing started20140612
Package count1

External sources

Source: openFDA. Public-domain (CC0).