Pristiq - 55154-4230-8 - (desvenlafaxine succinate)

Alphabetical Index


Drug Information of Pristiq

Product NDC: 55154-4230
Proprietary Name: Pristiq
Non Proprietary Name: desvenlafaxine succinate
Active Ingredient(s): 50    mg/1 & nbsp;   desvenlafaxine succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Pristiq

Product NDC: 55154-4230
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021992
Marketing Category: NDA
Start Marketing Date: 20080501

Package Information of Pristiq

Package NDC: 55154-4230-8
Package Description: 2700 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55154-4230-8)

NDC Information of Pristiq

NDC Code 55154-4230-8
Proprietary Name Pristiq
Package Description 2700 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55154-4230-8)
Product NDC 55154-4230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desvenlafaxine succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080501
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name DESVENLAFAXINE SUCCINATE
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 Pristiq


General Information