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Nafcillin

NDC 23155-906 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic nameNafcillin Sodium
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a/ Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090560
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsNAFCILLIN SODIUM (1 g/4mL)
Marketing started20250131
Package count1

External sources

Source: openFDA. Public-domain (CC0).