NDC 10019-079

BENDAMUSTINE HYDROCHLORIDE

Bendamustine Hydrochloride

BENDAMUSTINE HYDROCHLORIDE is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Bendamustine Hydrochloride.

Product ID10019-079_132b5560-e803-4112-ae4c-c8c607e674c4
NDC10019-079
Product TypeHuman Prescription Drug
Proprietary NameBENDAMUSTINE HYDROCHLORIDE
Generic NameBendamustine Hydrochloride
Dosage FormInjection
Route of AdministrationINTRAVENOUS
Marketing Start Date2022-12-15
Marketing CategoryNDA /
Application NumberNDA216078
Labeler NameBaxter Healthcare Corporation
Substance NameBENDAMUSTINE HYDROCHLORIDE
Active Ingredient Strength100 mg/1
Pharm ClassesAlkylating Activity [MoA], Alkylating Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 10019-079-01

1 VIAL, MULTI-DOSE in 1 CARTON (10019-079-01) > 1 INJECTION in 1 VIAL, MULTI-DOSE
Marketing Start Date2022-12-15
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "BENDAMUSTINE HYDROCHLORIDE" or generic name "Bendamustine Hydrochloride"

NDCBrand NameGeneric Name
10019-079BENDAMUSTINE HYDROCHLORIDEbendamustine hydrochloride
16729-250bendamustine hydrochloridebendamustine hydrochloride
16729-251bendamustine hydrochloridebendamustine hydrochloride
42367-520BENDAMUSTINE HYDROCHLORIDEbendamustine hydrochloride
42367-521BELRAPZObendamustine hydrochloride
63459-348Bendekabendamustine hydrochloride
63459-390TREANDABendamustine Hydrochloride
63459-391TREANDABendamustine Hydrochloride
71225-120VIVIMUSTABENDAMUSTINE HYDROCHLORIDE

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