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Venlafaxine Hydrochloride - 49349-234-02 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 49349-234
Proprietary Name: Venlafaxine Hydrochloride
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 Hydrochloride

Product NDC: 49349-234
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077653
Marketing Category: ANDA
Start Marketing Date: 20110502

Package Information of Venlafaxine Hydrochloride

Package NDC: 49349-234-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-234-02)

NDC Information of Venlafaxine Hydrochloride

NDC Code 49349-234-02
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-234-02)
Product NDC 49349-234
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110502
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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 Hydrochloride


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