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Venlafaxine Hydrochloride - 59762-0182-3 - (VENLAFAXINE HYDROCHLORIDE)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 59762-0182
Proprietary Name: Venlafaxine Hydrochloride
Non Proprietary Name: VENLAFAXINE HYDROCHLORIDE
Active Ingredient(s): 150    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: 59762-0182
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020699
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20110602

Package Information of Venlafaxine Hydrochloride

Package NDC: 59762-0182-3
Package Description: 100 BLISTER PACK in 1 CARTON (59762-0182-3) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Venlafaxine Hydrochloride

NDC Code 59762-0182-3
Proprietary Name Venlafaxine Hydrochloride
Package Description 100 BLISTER PACK in 1 CARTON (59762-0182-3) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 59762-0182
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VENLAFAXINE HYDROCHLORIDE
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110602
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 150
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