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venlafaxine - 65862-406-90 - (venlafaxine hydrochloride)

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Drug Information of venlafaxine

Product NDC: 65862-406
Proprietary Name: venlafaxine
Non Proprietary Name: venlafaxine hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   venlafaxine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of venlafaxine

Product NDC: 65862-406
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090555
Marketing Category: ANDA
Start Marketing Date: 20100407

Package Information of venlafaxine

Package NDC: 65862-406-90
Package Description: 90 TABLET in 1 BOTTLE (65862-406-90)

NDC Information of venlafaxine

NDC Code 65862-406-90
Proprietary Name venlafaxine
Package Description 90 TABLET in 1 BOTTLE (65862-406-90)
Product NDC 65862-406
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100407
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 50
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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