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AMPICILLIN

NDC 23155-916 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic nameAmpicillin Injection
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090354
Dosage form / routePOWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsAMPICILLIN SODIUM (1 g/g)
Marketing started20250131
Package count1

External sources

Source: openFDA. Public-domain (CC0).