Bendamustine Hydrochloride 10019-0079
Product NDC
10019-0079- Manufacturer
- Baxter Healthcare Corporation
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 15, 2022
- Listing Expires
- December 31, 2027
- Application
- NDA216078
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bendamustine Hydrochloride | 100 mg/1 |
Drug Class
Alkylating Activity [MoA]Alkylating Drug [EPC]
Packaging Options(1)
1 VIAL, MULTI-DOSE in 1 CARTON (10019-079-01) / 1 INJECTION in 1 VIAL, MULTI-DOSE