Bendamustine Hydrochloride 68001-0572
Product NDC
68001-0572- 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]
Packaging Options(1)
1 VIAL, SINGLE-DOSE in 1 CARTON (68001-572-41) / 20 mL in 1 VIAL, SINGLE-DOSE