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Venlafaxine Hydrochloride - 54868-4055-3 - (venlafaxine hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 54868-4055
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: 54868-4055
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078627
Marketing Category: ANDA
Start Marketing Date: 20070719

Package Information of Venlafaxine Hydrochloride

Package NDC: 54868-4055-3
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-4055-3)

NDC Information of Venlafaxine Hydrochloride

NDC Code 54868-4055-3
Proprietary Name Venlafaxine Hydrochloride
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-4055-3)
Product NDC 54868-4055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070719
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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