FDA NDC Directory · JSON-LD · Markdown

Cefuroxime

NDC 0143-9567 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065048
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFUROXIME SODIUM (1.5 g/1)
Marketing started20040109
Package count1

External sources

Source: openFDA. Public-domain (CC0).