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Venlafaxine Hydrochloride - 49349-818-02 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 49349-818
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: 49349-818
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022104
Marketing Category: NDA
Start Marketing Date: 20111117

Package Information of Venlafaxine Hydrochloride

Package NDC: 49349-818-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-818-02)

NDC Information of Venlafaxine Hydrochloride

NDC Code 49349-818-02
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-818-02)
Product NDC 49349-818
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111117
Marketing Category Name NDA
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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