| NDC Code | 65580-304-03 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65580-304-03) |
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| Product NDC | 65580-304 |
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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, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20080930 |
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| End Marketing Date | 20180731 |
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| Marketing Category Name | NDA |
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| Application Number | NDA022104 |
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| Manufacturer | Upstate Pharma, 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 and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
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