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Desvenlafaxine - 63304-191-90 - (Desvenlafaxine)

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Drug Information of Desvenlafaxine

Product NDC: 63304-191
Proprietary Name: Desvenlafaxine
Non Proprietary Name: Desvenlafaxine
Active Ingredient(s): 50    mg/1 & nbsp;   Desvenlafaxine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Desvenlafaxine

Product NDC: 63304-191
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA204150
Marketing Category: NDA
Start Marketing Date: 20130305

Package Information of Desvenlafaxine

Package NDC: 63304-191-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-191-90)

NDC Information of Desvenlafaxine

NDC Code 63304-191-90
Proprietary Name Desvenlafaxine
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-191-90)
Product NDC 63304-191
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desvenlafaxine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130305
Marketing Category Name NDA
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name DESVENLAFAXINE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Desvenlafaxine


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