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Cyclophosphamide

NDC 10019-955 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic namecyclophosphamide
Labeler / ManufacturerBaxter Healthcare Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA040745
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS ORAL
Active ingredientsCYCLOPHOSPHAMIDE (500 mg/25mL)
Marketing started20080521
Package count1

External sources

Source: openFDA. Public-domain (CC0).