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Cyclophosphamide

NDC 72603-326 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210046
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS ORAL
Active ingredientsCYCLOPHOSPHAMIDE (1 g/50mL)
Marketing started20190510
Marketing ended20260531
Package count1

External sources

Source: openFDA. Public-domain (CC0).