| NDC Code | 70710-1615-1 |
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| Package Description | 1 VIAL in 1 CARTON (70710-1615-1) > 5 mL in 1 VIAL |
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| Product NDC | 70710-1615 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fosaprepitant |
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| Non-Proprietary Name | Fosaprepitant |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20201101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212957 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | FOSAPREPITANT |
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| Strength | 150 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Neurokinin 1 Antagonists [MoA], Substance P/Neurokinin-1 Receptor Antagonist [EPC] |
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