TheraRadar
Data updated: May 26, 2026

QELBREE (viloxazine hydrochloride)

CNS Approved 2021-04-02

Qelbree is a medication used for Attention-Deficit Hyperactivity Disorder (ADHD) in adults and children 6 years of age and older. It helps patients with ADHD manage their symptoms by functioning as a selective norepinephrine reuptake inhibitor. This drug provides a therapeutic option for both pediatric and adult populations struggling with the condition.

Source: FDA Label • SUPERNUS PHARMS

How QELBREE Works

While the exact way viloxazine works is not fully known, it is thought to work by inhibiting the reuptake of norepinephrine. By blocking this reuptake, the drug is believed to help manage the symptoms associated with ADHD.

2
Indications
--
Phase 3 Trials
5
Years on Market

Details

Status
Prescription
First Approved
2021-04-02
Patent Cliff
2035

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Routes
ORAL
Dosage Forms
CAPSULE, EXTENDED RELEASE

Companies

Active Ingredient: VILOXAZINE HYDROCHLORIDE

QELBREE Approval History

2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
9 FDA actions from 2021 to 2025 · 1 indication expansions
Jan 2025 SUPPL
Label · Labeling
Apr 2022 SUPPL
Efficacy
Apr 2021 ORIGINAL
New Drug · Type 1 - New Molecular Entity

What QELBREE Treats

1 indications

QELBREE is approved for 1 conditions since its original approval in 2021. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Attention-Deficit Hyperactivity Disorder
Source: FDA Label

QELBREE Boxed Warning

SUICIDAL THOUGHTS AND BEHAVIORS In clinical studies, higher rates of suicidal thoughts and behavior were reported in patients with ADHD treated with Qelbree than in patients treated with placebo . Closely monitor all Qelbree-treated patients for clinical worsening, and for emergence of suicidal thoughts and behaviors [see Warnings and Precautions (5.1) ] . WARNING: SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning. In clinical trials, higher rates of sui...

QELBREE Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

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Active Pipeline

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

QELBREE FDA Label Details

Indications & Usage

FDA Label (PDF)

QELBREE is indicated for the treatment of Attention-Deficit Hyperactivity Disorder.

⚠️ BOXED WARNING

WARNING: SUICIDAL THOUGHTS AND BEHAVIORS In clinical studies, higher rates of suicidal thoughts and behavior were reported in patients with ADHD treated with Qelbree than in patients treated with placebo . Closely monitor all Qelbree-treated patients for clinical worsening, and for emergence of suic...

View full patent landscape →
6 OB patents · 2 families · 57 international docs across 8 countries

QELBREE Patents & Exclusivity

Latest Patent: Apr 2035
Exclusivity: Apr 2026

Patents (6 active)

US9662338 Expires Apr 2, 2035
US9603853 Expires Feb 7, 2033
US9358204 Expires Feb 7, 2033
US12121523 Expires Sep 4, 2029
US11458143 Expires Sep 4, 2029
US11324753 Expires Sep 4, 2029

Exclusivity

NCE Until Apr 2026
NCE Until Apr 2026
NCE Until Apr 2026
NCE Until Apr 2026
NCE Until Apr 2026
NCE Until Apr 2026
NCE Until Apr 2026
NCE Until Apr 2026
NCE Until Apr 2026
Source: FDA Orange Book

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Patent Timeline

  • Cliff: 2035
  • 54 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

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  • Same target/indication analysis
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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.