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Nafcillin

NDC 63323-327 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameNAFCILLIN SODIUM
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090002
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsNAFCILLIN SODIUM (1 g/4mL)
Marketing started20110630
Package count1

External sources

Source: openFDA. Public-domain (CC0).