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Effexor
Effexor - 0008-0837-22 - (VENLAFAXINE HYDROCHLORIDE)
Drug Information of Effexor
| Product NDC: | 0008-0837 |
| Proprietary Name: | Effexor |
| Non Proprietary Name: | VENLAFAXINE HYDROCHLORIDE |
| Active Ingredient(s): | 37.5 mg/1 & nbsp; VENLAFAXINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Effexor
| Product NDC: | 0008-0837 |
| Labeler Name: | Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020699 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19971101 |
Package Information of Effexor
| Package NDC: | 0008-0837-22 |
| Package Description: | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0837-22) |
NDC Information of Effexor
| NDC Code | 0008-0837-22 |
| Proprietary Name | Effexor |
| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0837-22) |
| Product NDC | 0008-0837 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VENLAFAXINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19971101 |
| Marketing Category Name | NDA |
| Labeler Name | Wyeth Pharmaceuticals Company, a subsidiary of Pfizer 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] |
