Pristiq - 35356-491-30 - (desvenlafaxine succinate)

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Drug Information of Pristiq

Product NDC: 35356-491
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: 35356-491
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021992
Marketing Category: NDA
Start Marketing Date: 20120416

Package Information of Pristiq

Package NDC: 35356-491-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (35356-491-30)

NDC Information of Pristiq

NDC Code 35356-491-30
Proprietary Name Pristiq
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (35356-491-30)
Product NDC 35356-491
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desvenlafaxine succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120416
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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