| NDC Code | 70518-2244-0 |
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| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2244-0) |
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| Product NDC | 70518-2244 |
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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 | 20190801 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204082 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | DESVENLAFAXINE SUCCINATE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA] |
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