NDC Code | 67457-325-12 |
Package Description | 5 mL in 1 VIAL, SINGLE-DOSE (67457-325-12) |
Product NDC | 67457-325 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bendamustine Hydrochloride |
Non-Proprietary Name | Bendamustine Hydrochloride |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20180426 |
Marketing Category Name | ANDA |
Application Number | ANDA204104 |
Manufacturer | Mylan Institutional LLC |
Substance Name | BENDAMUSTINE HYDROCHLORIDE |
Strength | 25 |
Strength Unit | mg/5mL |
Pharmacy Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |