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TREANDA

NDC 63459-391 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameBendamustine Hydrochloride
Labeler / ManufacturerCephalon, LLC
Marketing categoryNew Drug Application (innovator) · App NDA022249
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsBENDAMUSTINE HYDROCHLORIDE (100 mg/20mL)
Marketing started20080331
Package count1

External sources

Source: openFDA. Public-domain (CC0).