desvenlafaxine succinate

FDA Drug Profile — Pristiq Extended-Release, desvenlafaxine

desvenlafaxine succinate is listed in the FDA National Drug Code directory with 8 NDC codes, marketed under brand names including Pristiq Extended-Release, desvenlafaxine. Available dosage forms: tablet, extended release, powder.

Drug Details

Generic Name
desvenlafaxine succinate
Brand Names
Pristiq Extended-Release, desvenlafaxine
Application Number
NDA021992
Sponsor
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Codes
8
Dosage Forms
TABLET, EXTENDED RELEASE, POWDER
Routes
ORAL
Active Ingredients
DESVENLAFAXINE SUCCINATE

Indications and Usage

1 INDICATIONS AND USAGE Desvenlafaxine extended-release tablet is indicated for the treatment of adults with major depressive disorder (MDD) [see CLINICAL STUDIES ( 14 )]. Desvenlafaxine extended-release tablet, is a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of adults with major depressive disorder (MDD) ( 1 ).