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Venlafaxine Hydrochloride - 49349-913-02 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 49349-913
Proprietary Name: Venlafaxine Hydrochloride
Non Proprietary Name: Venlafaxine Hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   Venlafaxine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 49349-913
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020699
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120314

Package Information of Venlafaxine Hydrochloride

Package NDC: 49349-913-02
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (49349-913-02)

NDC Information of Venlafaxine Hydrochloride

NDC Code 49349-913-02
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (49349-913-02)
Product NDC 49349-913
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120314
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name REMEDYREPACK INC.
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 75
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


General Information