| NDC Code | 0093-7382-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (0093-7382-01) |
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| Product NDC | 0093-7382 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20060804 |
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| End Marketing Date | 20210430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076690 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | VENLAFAXINE HYDROCHLORIDE |
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| Strength | 75 |
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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] |
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