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VENLAFAXINE HYDROCHLORIDE - 55154-3382-0 - (VENLAFAXINE HYDROCHLORIDE)

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Drug Information of VENLAFAXINE HYDROCHLORIDE

Product NDC: 55154-3382
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): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of VENLAFAXINE HYDROCHLORIDE

Product NDC: 55154-3382
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078865
Marketing Category: ANDA
Start Marketing Date: 20110607

Package Information of VENLAFAXINE HYDROCHLORIDE

Package NDC: 55154-3382-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-3382-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of VENLAFAXINE HYDROCHLORIDE

NDC Code 55154-3382-0
Proprietary Name VENLAFAXINE HYDROCHLORIDE
Package Description 10 BLISTER PACK in 1 BAG (55154-3382-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-3382
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VENLAFAXINE HYDROCHLORIDE
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110607
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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