| NDC Code | 70436-029-80 |
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| Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 BOX (70436-029-80) |
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| Product NDC | 70436-029 |
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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 | 20190128 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211661 |
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| Manufacturer | Slate Run Pharmaceuticals |
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| Substance Name | VORICONAZOLE |
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| Strength | 200 |
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| Strength Unit | mg/1 |
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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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