| NDC Code | 0121-1091-55 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0121-1091-55) / 20 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 0121-1091 |
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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 Injection |
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| Dosage Form | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20260514 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA220043 |
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| Manufacturer | PAI Holdings, LLC dba PAI Pharma |
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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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