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Venlafaxine Hydrochloride - 63629-3323-1 - (Venlafaxine)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 63629-3323
Proprietary Name: Venlafaxine Hydrochloride
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 Hydrochloride

Product NDC: 63629-3323
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079098
Marketing Category: ANDA
Start Marketing Date: 20100511

Package Information of Venlafaxine Hydrochloride

Package NDC: 63629-3323-1
Package Description: 30 TABLET in 1 BOTTLE (63629-3323-1)

NDC Information of Venlafaxine Hydrochloride

NDC Code 63629-3323-1
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (63629-3323-1)
Product NDC 63629-3323
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100511
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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