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NAFCILLIN SODIUM

NDC 72485-405 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerArmas Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200002
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsNAFCILLIN SODIUM (1 g/1)
Marketing started20231101
Package count1

External sources

Source: openFDA. Public-domain (CC0).