| NDC Code | 0054-0401-22 |
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| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0054-0401-22) |
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| Product NDC | 0054-0401 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Desvenlafaxine |
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| Non-Proprietary Name | Desvenlafaxine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20170301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204083 |
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| Manufacturer | Hikma Pharmaceuticals USA Inc. |
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| Substance Name | DESVENLAFAXINE SUCCINATE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
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