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FDA accepts Jazz Pharma's solriamfetol application for excessive sleepiness in patients with narcolepsy or obstructive sleep apnea

Published 03/02/2018, 08:51 AM
© Reuters.  FDA accepts Jazz Pharma's solriamfetol application for excessive sleepiness in patients with narcolepsy or obstructive sleep apnea
JAZZ
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  • The FDA accepts for review Jazz Pharmaceuticals ' (NASDAQ:JAZZ) marketing application seeking approval for solriamfetol for the treatment of excessive sleepiness in adult patients with narcolepsy or obstructive sleep apnea. The agency's action date is December 20.
  • Solriamfetol is a selective dopamine and norepinephrine reuptake inhibitor licensed from Aerial Biopharma in 2014.
  • Previously: Jazz Pharma submits U.S. marketing application for solriamfetol (Dec. 21, 2017)
  • Now read: ROTY Volume 1 Edition 83: Thank You For Your Patience - Launch Day Has Arrived!


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