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Viloxazine Hydrochloride bulk supplier for pharma manufacturers

Viloxazine Hydrochloride 100 mg, 150 mg, 200 mg Suppliers & Bulk Manufacturers

Available Forms: Capsules

Available Strengths: 100 mg, 150 mg, 200 mg

Reference Brands: Qelbree (USA)

Category: Neurology

Viloxazine extended-release capsules (100–200 mg) are a non-stimulant treatment for ADHD in children and adults, acting mainly as a noradrenaline reuptake inhibitor. It is not a controlled substance. It is made by Supernus as Qelbree. Supply is through authorised distribution or named-patient import; ask us which route fits your country.

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Product Description:

Viloxazine is a centrally acting selective norepinephrine reuptake inhibitor that is marketed under the brand name Qelbree, among others, for the treatment of attention deficit hyperactivity disorder (ADHD) in both children and adults. ADHD is a neurodevelopmental condition characterized by inattention, hyperactivity, and impulsivity, which can significantly impact academic performance, work productivity, and social functioning.

Viloxazine has a long clinical history and was originally marketed for nearly three decades as an antidepressant for the treatment of depressive disorders before its discontinuation for that indication. Based on its mechanism of action and effects on norepinephrine signaling in the brain, it was later repurposed and developed for the management of ADHD. In its current approved use, viloxazine is administered orally as an extended-release formulation, allowing for sustained drug release and once-daily dosing.

The extended-release form is designed to provide steady symptom control throughout the day while offering a non-stimulant alternative for patients who may not tolerate or respond well to stimulant medications. Although clinical evidence suggests that viloxazine may be less effective in reducing ADHD symptoms compared to stimulant therapies such as methylphenidate, it remains a valuable treatment option for selected patients seeking non-stimulant management of ADHD.

How Viloxazine Hydrochloride is supplied today, and licensing ahead of patent expiry

Named-patient import Where a patient needs the product in a market where it is not registered, named-patient import is the lawful route. It requires the treating physician's documentation and authorisation from the destination regulator. We handle this pathway. Named-patient access
Authorised distribution For registered markets, supply runs through the manufacturer's authorised distribution channel. We can identify the authorised route for your market and tell you whether the product is registered there at all. Innovator sourcing
A genericised alternative Where the clinical requirement is the drug class rather than this specific molecule, there is often an off-patent alternative that is faster to register and materially cheaper. Tell us the indication and target market and we will say plainly whether one exists. Discuss alternatives
Licensing and generic development Patents expire country by country, and in many countries development and dossier filing can start before expiry under research and regulatory-review exemptions. We connect manufacturers developing this molecule, dossier holders, licensees and tech-transfer partners for markets where it is, or will become, off-patent. Partner on this molecule
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Frequently Asked Questions

Viloxazine hydrochloride is used for the treatment of attention-deficit/hyperactivity disorder (ADHD) in pediatric and adult patients, helping to improve attention, focus, and behavioral control.

Viloxazine hydrochloride is a synthetic chemical compound formulated as a hydrochloride salt to improve stability, solubility, and oral absorption.

The trade name of viloxazine hydrochloride is Qelbree.

Qelbree is manufactured and marketed by Supernus Pharmaceuticals, Inc. in the United States.

The complete generic name is viloxazine hydrochloride.

The brand name is Qelbree.

Viloxazine hydrochloride finished dosage forms are manufactured in FDA-approved pharmaceutical facilities for the U.S. market, with manufacturing locations disclosed by the marketing authorization holder in regulatory submissions.

100–400 mg once daily for children and 200–600 mg for adults, depending on age and response.

No. Unlike stimulant ADHD medicines, it is not controlled, which simplifies prescribing and import.

Like other ADHD non-stimulants, it carries a warning about suicidal thoughts in young people.

Qelbree (Viloxazine ER) is developed and sold by Supernus Pharmaceuticals. PharmaTradz handles enquiries for authorised supply of the originator product, named-patient import where it is not registered, and licensing or development work ahead of patent expiry.

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