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Ampicillin

NDC 0781-9407 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic nameAmpicillin sodium
Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA061395
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsAMPICILLIN SODIUM (500 mg/1)
Marketing started19710303
Package count0

External sources

Source: openFDA. Public-domain (CC0).