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Mitoxantrone

NDC 63323-132 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameMITOXANTRONE HYDROCHLORIDE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077496
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMITOXANTRONE HYDROCHLORIDE (2 mg/mL)
Marketing started20060411
Package count3

External sources

Source: openFDA. Public-domain (CC0).