Product NDC: | 55154-4218 |
Proprietary Name: | Effexor |
Non Proprietary Name: | venlafaxine hydrochloride |
Active Ingredient(s): | 75 mg/1 & nbsp; venlafaxine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4218 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020699 |
Marketing Category: | NDA |
Start Marketing Date: | 19971101 |
Package NDC: | 55154-4218-2 |
Package Description: | 3780 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55154-4218-2) |
NDC Code | 55154-4218-2 |
Proprietary Name | Effexor |
Package Description | 3780 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55154-4218-2) |
Product NDC | 55154-4218 |
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 | Cardinal Health |
Substance Name | VENLAFAXINE HYDROCHLORIDE |
Strength Number | 75 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |