Bendamustine Hydrochloride 68001-0572-41

Package NDC

68001-0572-41

Manufacturer: Bluepoint Laboratories
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: September 15, 2023
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]

Selected Package

68001-0572-41Selected

1 VIAL, SINGLE-DOSE in 1 CARTON (68001-572-41) / 20 mL in 1 VIAL, SINGLE-DOSE