Effexor - 49999-249-30 - (venlafaxine hydrochloride)

Alphabetical Index


Drug Information of Effexor

Product NDC: 49999-249
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)

Labeler Information of Effexor

Product NDC: 49999-249
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020699
Marketing Category: NDA
Start Marketing Date: 20110131

Package Information of Effexor

Package NDC: 49999-249-30
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-249-30)

NDC Information of Effexor

NDC Code 49999-249-30
Proprietary Name Effexor
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-249-30)
Product NDC 49999-249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110131
Marketing Category Name NDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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]

Complete Information of Effexor


General Information