| 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] |