FDA NDC Directory · JSON-LD · Markdown

Cefazolin

NDC 0143-9983 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065143
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFAZOLIN SODIUM (10 g/1)
Marketing started20041018
Package count1

External sources

Source: openFDA. Public-domain (CC0).