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Ampicillin

NDC 65219-014 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic nameampicillin sodium
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA062719
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsAMPICILLIN SODIUM (250 mg/1)
Marketing started20191030
Package count1

External sources

Source: openFDA. Public-domain (CC0).