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Ifosfamide

NDC 63323-142 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameIFOSFAMIDE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076078
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsIFOSFAMIDE (1 g/1)
Marketing started20030128
Package count1

External sources

Source: openFDA. Public-domain (CC0).