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Nafcillin

NDC 63323-330 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic nameNAFCILLIN
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090005
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsNAFCILLIN SODIUM (10 g/100mL)
Marketing started20110427
Package count1

External sources

Source: openFDA. Public-domain (CC0).