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Heparin Sodium

NDC 68083-136 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA205323
Dosage form / routeINJECTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsHEPARIN SODIUM (5000 [USP'U]/mL)
Marketing started20170309
Package count1

External sources

Source: openFDA. Public-domain (CC0).