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venlafaxine
venlafaxine - 65862-406-90 - (venlafaxine hydrochloride)
Drug Information of venlafaxine
| Product NDC: | 65862-406 |
| Proprietary Name: | venlafaxine |
| Non Proprietary Name: | venlafaxine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; venlafaxine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of venlafaxine
| Product NDC: | 65862-406 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090555 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100407 |
Package Information of venlafaxine
| Package NDC: | 65862-406-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (65862-406-90) |
NDC Information of venlafaxine
| NDC Code | 65862-406-90 |
| Proprietary Name | venlafaxine |
| Package Description | 90 TABLET in 1 BOTTLE (65862-406-90) |
| Product NDC | 65862-406 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | venlafaxine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100407 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
