FDA Approves Supernus's Qelbree For Treatment Of Attention-deficit Hyperactivity Disorder
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FDA Approves Supernus's Qelbree For Treatment Of Attention-deficit Hyperactivity Disorder
(RTTNews) - Supernus Pharmaceuticals Inc. (SUPN) said that the U.S. Food and Drug Administration approved Qelbree or viloxazine extended-release capsules for the treatment of attention-deficit hyperactivity disorder or ADHD in pediatric patients 6 to 17 years of age.Supernus pla
Apr 3, 2021
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New drug for children with ADHD approved by FDA
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Qelbree is the first non-stimulant ADHD-specific drug to receive FDA approval in almost 20 years. It is dubbed as the faster version of Eli Lilly’s non-stimulant Strattera, sales of which have been on the decline since it went off patent in 2017. Find out more: https://buff.ly/3mvlbOW #ADHD #NonStimulants #Qelbree #Stimulants | Xtalks Webinars | Facebook
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