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Enoxaparin Sodium

NDC 71288-426 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214856
Dosage form / routeINJECTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsENOXAPARIN SODIUM (300 mg/3mL)
Marketing started20220614
Package count1

External sources

Source: openFDA. Public-domain (CC0).