NDC Code | 24338-270-01 |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (24338-270-01) / 4 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 24338-270 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Vivimusta |
Non-Proprietary Name | Bendamustine Hydrochloride |
Dosage Form | INJECTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20250401 |
Marketing Category Name | NDA |
Application Number | NDA212209 |
Manufacturer | Azurity Pharmaceuticals, Inc. |
Substance Name | BENDAMUSTINE HYDROCHLORIDE |
Strength | 25 |
Strength Unit | mg/mL |
Pharmacy Classes | Alkylating Activity [MoA], Alkylating Drug [EPC] |