Bendamustine Hydrochloride 16729-0251

Product NDC

16729-0251

Manufacturer: Accord Healthcare, Inc.
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: December 7, 2022
Listing Expires: December 31, 2026
Application: ANDA205574

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Active Ingredients

Ingredient	Strength
Bendamustine Hydrochloride	100 mg/20mL

Drug Class

Alkylating Activity [MoA]Alkylating Drug [EPC]

Packaging Options(1)

16729-0251-05

1 VIAL, SINGLE-DOSE in 1 CARTON (16729-251-05) / 20 mL in 1 VIAL, SINGLE-DOSE

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