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Venlafaxine Hydrochloride - 52959-890-90 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 52959-890
Proprietary Name: Venlafaxine Hydrochloride
Non Proprietary Name: Venlafaxine Hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   Venlafaxine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 52959-890
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077653
Marketing Category: ANDA
Start Marketing Date: 20080613

Package Information of Venlafaxine Hydrochloride

Package NDC: 52959-890-90
Package Description: 90 TABLET in 1 BOTTLE (52959-890-90)

NDC Information of Venlafaxine Hydrochloride

NDC Code 52959-890-90
Proprietary Name Venlafaxine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (52959-890-90)
Product NDC 52959-890
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080613
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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 Hydrochloride


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