| NDC Code | 65219-190-30 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (65219-190-30) / 20 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 65219-190 |
|---|
| 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 | 20201201 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211099 |
|---|
| Manufacturer | Fresenius Kabi USA, LLC |
|---|
| 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] |
|---|