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BENDAMUSTINE HYDROCHLORIDE

NDC 10019-079 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namebendamustine hydrochloride
Labeler / ManufacturerBaxter Healthcare Corporation
Marketing categoryNew Drug Application (innovator) · App NDA216078
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsBENDAMUSTINE HYDROCHLORIDE (100 mg/1)
Marketing started20221215
Package count1

External sources

Source: openFDA. Public-domain (CC0).