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venlafaxine - 16714-314-01 - (venlafaxine)

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Drug Information of venlafaxine

Product NDC: 16714-314
Proprietary Name: venlafaxine
Non Proprietary Name: venlafaxine
Active Ingredient(s): 75    mg/1 & nbsp;   venlafaxine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of venlafaxine

Product NDC: 16714-314
Labeler Name: NorthStar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078932
Marketing Category: ANDA
Start Marketing Date: 20101221

Package Information of venlafaxine

Package NDC: 16714-314-01
Package Description: 100 TABLET in 1 BOTTLE (16714-314-01)

NDC Information of venlafaxine

NDC Code 16714-314-01
Proprietary Name venlafaxine
Package Description 100 TABLET in 1 BOTTLE (16714-314-01)
Product NDC 16714-314
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name venlafaxine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101221
Marketing Category Name ANDA
Labeler Name NorthStar RxLLC
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


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