Effexor - 54868-4252-0 - (venlafaxine hydrochloride)

Alphabetical Index


Drug Information of Effexor

Product NDC: 54868-4252
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: 54868-4252
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020699
Marketing Category: NDA
Start Marketing Date: 20010828

Package Information of Effexor

Package NDC: 54868-4252-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4252-0)

NDC Information of Effexor

NDC Code 54868-4252-0
Proprietary Name Effexor
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4252-0)
Product NDC 54868-4252
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20010828
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
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