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Venlafaxine - 68382-019-05 - (Venlafaxine)

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Drug Information of Venlafaxine

Product NDC: 68382-019
Proprietary Name: Venlafaxine
Non Proprietary Name: Venlafaxine
Active Ingredient(s): 37.5    mg/1 & nbsp;   Venlafaxine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine

Product NDC: 68382-019
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077653
Marketing Category: ANDA
Start Marketing Date: 20080613

Package Information of Venlafaxine

Package NDC: 68382-019-05
Package Description: 500 TABLET in 1 BOTTLE (68382-019-05)

NDC Information of Venlafaxine

NDC Code 68382-019-05
Proprietary Name Venlafaxine
Package Description 500 TABLET in 1 BOTTLE (68382-019-05)
Product NDC 68382-019
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080613
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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 Venlafaxine


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