Effexor - 63629-3314-1 - (VENLAFAXINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Effexor

Product NDC: 63629-3314
Proprietary Name: Effexor
Non Proprietary Name: VENLAFAXINE HYDROCHLORIDE
Active Ingredient(s): 150    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: 63629-3314
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020699
Marketing Category: NDA
Start Marketing Date: 19971101

Package Information of Effexor

Package NDC: 63629-3314-1
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-3314-1)

NDC Information of Effexor

NDC Code 63629-3314-1
Proprietary Name Effexor
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-3314-1)
Product NDC 63629-3314
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 Bryant Ranch Prepack
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 150
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