FDA NDC Directory · JSON-LD · Markdown

AMPICILLIN

NDC 51662-1595 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA062719
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsAMPICILLIN SODIUM (250 mg/1)
Marketing started20220818
Package count1

External sources

Source: openFDA. Public-domain (CC0).