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Cefepime Hydrochloride

NDC 0143-9382 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214402
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFEPIME HYDROCHLORIDE (1 g/1)
Marketing started20250922
Package count1

External sources

Source: openFDA. Public-domain (CC0).