| NDC Code | 72843-441-01 |
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| Package Description | 20 mL in 1 VIAL, SINGLE-USE (72843-441-01) |
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| Product NDC | 72843-441 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Voriconazole |
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| Non-Proprietary Name | Voriconazole |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20200831 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211264 |
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| Manufacturer | UBI Pharma Inc. |
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| Substance Name | VORICONAZOLE |
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| Strength | 10 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA] |
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