Drugplain

NDC 16729-250-03

bendamustine hydrochloride 25 mg/5mL

bendamustine hydrochloride · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

No Recall History

bendamustine hydrochloride is a injection, powder, lyophilized, for solution containing bendamustine hydrochloride at a strength of 25 mg/5mL. Manufactured by Accord Healthcare, Inc..

Key Facts

Brand Name
bendamustine hydrochloride
Generic Name
bendamustine hydrochloride
NDC Code (Package)
16729-250-03
NDC Code (Product)
16729-250
Manufacturer
Accord Healthcare, Inc.
Strength
25 mg/5mL
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Marketing Status
Application #
ANDA205574
Marketing Start
12/07/2022

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.