Effexor - 0008-0837-20 - (VENLAFAXINE HYDROCHLORIDE)

Alphabetical Index


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: 0008-0837-20
Package Description: 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0837-20)

NDC Information of Effexor

NDC Code 0008-0837-20
Proprietary Name Effexor
Package Description 15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0837-20)
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]

Complete Information of Effexor


General Information