FDA NDC Directory · JSON-LD · Markdown

Ampicillin

NDC 65219-016 · 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 (500 mg/1)
Marketing started20200803
Package count1

External sources

Source: openFDA. Public-domain (CC0).