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Venlafaxine Hydrochloride - 49349-930-02 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 49349-930
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): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 49349-930
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091272
Marketing Category: ANDA
Start Marketing Date: 20130411

Package Information of Venlafaxine Hydrochloride

Package NDC: 49349-930-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-930-02)

NDC Information of Venlafaxine Hydrochloride

NDC Code 49349-930-02
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-930-02)
Product NDC 49349-930
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130411
Marketing Category Name ANDA
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


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