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Heparin Sodium

NDC 71288-449 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211007
Dosage form / routeINJECTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsHEPARIN SODIUM (1000 [USP'U]/mL)
Marketing started20250702
Package count1

External sources

Source: openFDA. Public-domain (CC0).