NDC Code | 72266-131-01 |
Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (72266-131-01) / 20 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 72266-131 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Voriconazole |
Non-Proprietary Name | Voriconazole |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20210104 |
Marketing Category Name | ANDA |
Application Number | ANDA211099 |
Manufacturer | Fosun Pharma USA Inc. |
Substance Name | VORICONAZOLE |
Strength | 10 |
Strength Unit | mg/mL |
Pharmacy Classes | Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA] |