| NDC Code | 71288-103-20 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-103-20) / 20 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 71288-103 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Bendamustine |
|---|
| Non-Proprietary Name | Bendamustine Hcl |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20230605 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211001 |
|---|
| Manufacturer | Meitheal Pharmaceuticals Inc. |
|---|
| Substance Name | BENDAMUSTINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/20mL |
|---|
| Pharmacy Classes | Alkylating Activity [MoA], Alkylating Drug [EPC] |
|---|