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Venlafaxine Hydrochloride - 42291-895-90 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 42291-895
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
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine Hydrochloride

Product NDC: 42291-895
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079098
Marketing Category: ANDA
Start Marketing Date: 20120507

Package Information of Venlafaxine Hydrochloride

Package NDC: 42291-895-90
Package Description: 90 TABLET in 1 BOTTLE (42291-895-90)

NDC Information of Venlafaxine Hydrochloride

NDC Code 42291-895-90
Proprietary Name Venlafaxine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (42291-895-90)
Product NDC 42291-895
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120507
Marketing Category Name ANDA
Labeler Name AvKARE, 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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