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Venlafaxine - 23155-249-07 - (Venlafaxine)

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Drug Information of Venlafaxine

Product NDC: 23155-249
Proprietary Name: Venlafaxine
Non Proprietary Name: Venlafaxine
Active Ingredient(s): 75    mg/1 & nbsp;   Venlafaxine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine

Product NDC: 23155-249
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079009
Marketing Category: ANDA
Start Marketing Date: 20121130

Package Information of Venlafaxine

Package NDC: 23155-249-07
Package Description: 20 TABLET in 1 BOTTLE (23155-249-07)

NDC Information of Venlafaxine

NDC Code 23155-249-07
Proprietary Name Venlafaxine
Package Description 20 TABLET in 1 BOTTLE (23155-249-07)
Product NDC 23155-249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121130
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
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 Venlafaxine


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