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Ampicillin

NDC 83270-315 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerONESOURCE SPECIALTY PHARMA LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA202198
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsAMPICILLIN SODIUM (10 g/1)
Marketing started20260227
Package count1

External sources

Source: openFDA. Public-domain (CC0).