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Ampicillin Sodium

NDC 25021-197 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA201404
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsAMPICILLIN SODIUM (10 g/100mL)
Marketing started20250115
Package count1

External sources

Source: openFDA. Public-domain (CC0).