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Venlafaxine Hydrochloride - 0131-3267-32 - (venlafaxine hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 0131-3267
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): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 0131-3267
Labeler Name: Schwarz Pharma Manufacturing, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022104
Marketing Category: NDA
Start Marketing Date: 20100429

Package Information of Venlafaxine Hydrochloride

Package NDC: 0131-3267-32
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0131-3267-32)

NDC Information of Venlafaxine Hydrochloride

NDC Code 0131-3267-32
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0131-3267-32)
Product NDC 0131-3267
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100429
Marketing Category Name NDA
Labeler Name Schwarz Pharma Manufacturing, Inc.
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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