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Venlafaxine Hydrochloride
Venlafaxine Hydrochloride - 41616-760-88 - (Venlafaxine Hydrochloride)
Drug Information of Venlafaxine Hydrochloride
| Product NDC: | 41616-760 |
| Proprietary Name: | Venlafaxine Hydrochloride |
| Non Proprietary Name: | Venlafaxine Hydrochloride |
| Active Ingredient(s): | 37.5 mg/1 & nbsp; Venlafaxine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Venlafaxine Hydrochloride
| Product NDC: | 41616-760 |
| Labeler Name: | Sun Pharma Global Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091272 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100818 |
Package Information of Venlafaxine Hydrochloride
| Package NDC: | 41616-760-88 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (41616-760-88) |
NDC Information of Venlafaxine Hydrochloride
| NDC Code | 41616-760-88 |
| Proprietary Name | Venlafaxine Hydrochloride |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (41616-760-88) |
| Product NDC | 41616-760 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Venlafaxine Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100818 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global Inc. |
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
| Strength Number | 37.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
