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Venlafaxine Hydrochloride - 21695-719-30 - (Venlafaxine Hydrochloride)

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Drug Information of Venlafaxine Hydrochloride

Product NDC: 21695-719
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: 21695-719
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076690
Marketing Category: ANDA
Start Marketing Date: 20090903

Package Information of Venlafaxine Hydrochloride

Package NDC: 21695-719-30
Package Description: 30 TABLET in 1 BOTTLE (21695-719-30)

NDC Information of Venlafaxine Hydrochloride

NDC Code 21695-719-30
Proprietary Name Venlafaxine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (21695-719-30)
Product NDC 21695-719
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090903
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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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