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Venlafaxine Hydrochloride - 65841-672-05 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 65841-672
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
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 65841-672
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077653
Marketing Category: ANDA
Start Marketing Date: 20080613

Package Information of Venlafaxine Hydrochloride

Package NDC: 65841-672-05
Package Description: 500 TABLET in 1 BOTTLE (65841-672-05)

NDC Information of Venlafaxine Hydrochloride

NDC Code 65841-672-05
Proprietary Name Venlafaxine Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (65841-672-05)
Product NDC 65841-672
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 Cadila Healthcare Limited
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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