NDC Code | 72338-200-01 |
Package Description | 1 VIAL in 1 CARTON (72338-200-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
Product NDC | 72338-200 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bortezomib |
Non-Proprietary Name | Bortezomib |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20180619 |
Marketing Category Name | ANDA |
Application Number | ANDA211898 |
Manufacturer | Waverley Pharma Inc |
Substance Name | BORTEZOMIB |
Strength | 3.5 |
Strength Unit | mg/1 |
Pharmacy Classes | Proteasome Inhibitor [EPC], Proteasome Inhibitors [MoA] |