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Venlafaxine Hydrochloride - 0603-6157-25 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 0603-6157
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: 0603-6157
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090027
Marketing Category: ANDA
Start Marketing Date: 20100804

Package Information of Venlafaxine Hydrochloride

Package NDC: 0603-6157-25
Package Description: 300 TABLET in 1 BOTTLE, PLASTIC (0603-6157-25)

NDC Information of Venlafaxine Hydrochloride

NDC Code 0603-6157-25
Proprietary Name Venlafaxine Hydrochloride
Package Description 300 TABLET in 1 BOTTLE, PLASTIC (0603-6157-25)
Product NDC 0603-6157
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100804
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
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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