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US FDA Approves Desvenlafaxine for the Treatment of Major Depressive Disorder
Friday, 07 March 2008
Wyeth received the US Food and Drug Administration(FDA) approval for Desvenlafaxine succinate (Pristiq™ ) a novel, once-daily serotonin-norepinephrine reuptake inhibitor (SNRI),for  the treatment of adult patients with major depressive disorder (MDD).