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Venlafaxine Hydrochloride - 41616-760-88 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 41616-760
Proprietary Name: Venlafaxine Hydrochloride
Non Proprietary Name: Venlafaxine Hydrochloride
Active Ingredient(s): 37.5    mg/1 & nbsp;   Venlafaxine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 41616-760
Labeler Name: Sun Pharma Global Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091272
Marketing Category: ANDA
Start Marketing Date: 20100818

Package Information of Venlafaxine Hydrochloride

Package NDC: 41616-760-88
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (41616-760-88)

NDC Information of Venlafaxine Hydrochloride

NDC Code 41616-760-88
Proprietary Name Venlafaxine Hydrochloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (41616-760-88)
Product NDC 41616-760
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100818
Marketing Category Name ANDA
Labeler Name Sun Pharma Global 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 Hydrochloride


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