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Venlafaxine Hydrochloride - 65862-529-10 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 65862-529
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: 65862-529
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200834
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of Venlafaxine Hydrochloride

Package NDC: 65862-529-10
Package Description: 10 BLISTER PACK in 1 CARTON (65862-529-10) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Venlafaxine Hydrochloride

NDC Code 65862-529-10
Proprietary Name Venlafaxine Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (65862-529-10) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 65862-529
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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


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