NDC Code | 60505-6101-4 |
Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6101-4) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
Product NDC | 60505-6101 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bivalirudin |
Non-Proprietary Name | Bivalirudin |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20170717 |
End Marketing Date | 20210301 |
Marketing Category Name | ANDA |
Application Number | ANDA204876 |
Manufacturer | Apotex corp |
Substance Name | BIVALIRUDIN |
Strength | 250 |
Strength Unit | mg/1 |
Pharmacy Classes | Anti-coagulant [EPC],Direct Thrombin Inhibitor [EPC],Thrombin Inhibitors [MoA] |