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Venlafaxine hydrochloride - 55111-546-05 - (Venlafaxine hydrochloride)

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Drug Information of Venlafaxine hydrochloride

Product NDC: 55111-546
Proprietary Name: Venlafaxine hydrochloride
Non Proprietary Name: Venlafaxine hydrochloride
Active Ingredient(s): 37.5    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: 55111-546
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078301
Marketing Category: ANDA
Start Marketing Date: 20080616

Package Information of Venlafaxine hydrochloride

Package NDC: 55111-546-05
Package Description: 500 TABLET in 1 BOTTLE (55111-546-05)

NDC Information of Venlafaxine hydrochloride

NDC Code 55111-546-05
Proprietary Name Venlafaxine hydrochloride
Package Description 500 TABLET in 1 BOTTLE (55111-546-05)
Product NDC 55111-546
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080616
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 37.5
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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