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CEFAZOLIN

NDC 63323-237 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic nameCEFAZOLIN SODIUM
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065303
Dosage form / routePOWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFAZOLIN SODIUM (1 g/3mL)
Marketing started20110715
Package count1

External sources

Source: openFDA. Public-domain (CC0).