FDA NDC Directory · JSON-LD · Markdown

Cefuroxime sodium

NDC 25021-119 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA064125
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFUROXIME SODIUM (1.5 g/20mL)
Marketing started20160901
Package count1

External sources

Source: openFDA. Public-domain (CC0).