| NDC Code | 13811-715-90 |
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| Package Description | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-715-90) |
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| Product NDC | 13811-715 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Venlafaxine Hydrochloride |
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| Non-Proprietary Name | Venlafaxine Hydrochloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20100429 |
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| End Marketing Date | 20260930 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA022104 |
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| Manufacturer | Trigen Laboratories, LLC |
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| Substance Name | VENLAFAXINE HYDROCHLORIDE |
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| Strength | 225 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
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