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See the DrugPatentWatch profile for Qelbree
Qelbree (viloxazine) was approved by the U.S. Food and Drug Administration (FDA) on April 20, 2021 [1].
Qelbree is indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) in pediatric patients aged 6 to 17 years [1].
The active ingredient in Qelbree is viloxazine [1].
Viloxazine, under the brand name Qelbree, became available following its FDA approval in April 2021 [1].
The exact mechanism by which viloxazine exerts its therapeutic effects in ADHD is not fully understood, but it is believed to involve the potentiation of norepinephrine signaling in the brain by acting as a selective norepinephrine reuptake inhibitor [1].
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