| NDC Code | 60687-607-21 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-607-21) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-607-11) |
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| Product NDC | 60687-607 |
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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 | 20211201 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204082 |
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| Manufacturer | American Health Packaging |
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| Substance Name | DESVENLAFAXINE SUCCINATE |
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| Strength | 50 |
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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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