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Cefazolin

NDC 44567-708 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerWG Critical Care, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065306
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFAZOLIN SODIUM (10 g/1)
Marketing started20150306
Package count1

External sources

Source: openFDA. Public-domain (CC0).