| NDC Code | 41616-759-18 |
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| Package Description | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (41616-759-18) |
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| Product NDC | 41616-759 |
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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 | 20100818 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091272 |
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| Manufacturer | Sun Pharma Global 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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