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Last Updated: April 18, 2024

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QELBREE Drug Patent Profile


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When do Qelbree patents expire, and what generic alternatives are available?

Qelbree is a drug marketed by Supernus Pharms and is included in one NDA. There are five patents protecting this drug.

This drug has twenty-one patent family members in seven countries.

The generic ingredient in QELBREE is viloxazine hydrochloride. One supplier is listed for this compound. Additional details are available on the viloxazine hydrochloride profile page.

DrugPatentWatch® Generic Entry Outlook for Qelbree

Qelbree will be eligible for patent challenges on April 2, 2025. This date may extended up to six months if a pediatric exclusivity extension is applied to the drug's patents.

By analyzing the patents and regulatory protections it appears that the earliest date for generic entry will be February 7, 2033. This may change due to patent challenges or generic licensing.

Indicators of Generic Entry

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  Try a Trial

Summary for QELBREE
International Patents:21
US Patents:5
Applicants:1
NDAs:1
Finished Product Suppliers / Packagers: 1
Raw Ingredient (Bulk) Api Vendors: 89
Patent Applications: 134
Drug Prices: Drug price information for QELBREE
What excipients (inactive ingredients) are in QELBREE?QELBREE excipients list
DailyMed Link:QELBREE at DailyMed
Drug patent expirations by year for QELBREE
Drug Prices for QELBREE

See drug prices for QELBREE

DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for QELBREE
Generic Entry Date for QELBREE*:
Constraining patent/regulatory exclusivity:
NDA:
Dosage:
CAPSULE, EXTENDED RELEASE;ORAL

*The generic entry opportunity date is the latter of the last compound-claiming patent and the last regulatory exclusivity protection. Many factors can influence early or later generic entry. This date is provided as a rough estimate of generic entry potential and should not be used as an independent source.

Anatomical Therapeutic Chemical (ATC) Classes for QELBREE

US Patents and Regulatory Information for QELBREE

QELBREE is protected by five US patents and two FDA Regulatory Exclusivities.

Based on analysis by DrugPatentWatch, the earliest date for a generic version of QELBREE is ⤷  Try a Trial.

This potential generic entry date is based on patent ⤷  Try a Trial.

Generics may enter earlier, or later, based on new patent filings, patent extensions, patent invalidation, early generic licensing, generic entry preferences, and other factors.

Patents protecting QELBREE

Method of treatment of attention deficit/hyperactivity disorder (ADHD)
Patent Number: ⤷  Try a Trial
Patent Expiration: ⤷  Try a Trial
Patented Use: FOR THE TREATMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)


Patent Number: ⤷  Try a Trial
Patent Expiration: ⤷  Try a Trial
Patented Use: FOR THE TREATMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)

Formulations of viloxazine
Patent Number: ⤷  Try a Trial
Patent Expiration: ⤷  Try a Trial

Formulations of viloxazine
Patent Number: ⤷  Try a Trial
Patent Expiration: ⤷  Try a Trial
Patented Use: FOR THE TREATMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)

Formulations of viloxazine
Patent Number: ⤷  Try a Trial
Patent Expiration: ⤷  Try a Trial

FDA Regulatory Exclusivity protecting QELBREE

NEW CHEMICAL ENTITY
Exclusivity Expiration: ⤷  Try a Trial

NEW PATIENT POPULATION
Exclusivity Expiration: ⤷  Try a Trial

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Supernus Pharms QELBREE viloxazine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 211964-001 Apr 2, 2021 RX Yes No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Supernus Pharms QELBREE viloxazine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 211964-003 Apr 2, 2021 RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial Y ⤷  Try a Trial
Supernus Pharms QELBREE viloxazine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 211964-001 Apr 2, 2021 RX Yes No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Supernus Pharms QELBREE viloxazine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 211964-001 Apr 2, 2021 RX Yes No ⤷  Try a Trial ⤷  Try a Trial Y ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

International Patents for QELBREE

When does loss-of-exclusivity occur for QELBREE?

Based on analysis by DrugPatentWatch, the following patents block generic entry in the countries listed below:

Australia

Patent: 13217013
Estimated Expiration: ⤷  Try a Trial

Patent: 17206245
Estimated Expiration: ⤷  Try a Trial

Patent: 19216707
Estimated Expiration: ⤷  Try a Trial

Patent: 20233746
Estimated Expiration: ⤷  Try a Trial

Canada

Patent: 64088
Estimated Expiration: ⤷  Try a Trial

European Patent Office

Patent: 12074
Estimated Expiration: ⤷  Try a Trial

Patent: 33915
Estimated Expiration: ⤷  Try a Trial

Japan

Patent: 90100
Estimated Expiration: ⤷  Try a Trial

Patent: 10093
Estimated Expiration: ⤷  Try a Trial

Patent: 32973
Estimated Expiration: ⤷  Try a Trial

Patent: 15506980
Estimated Expiration: ⤷  Try a Trial

Patent: 18090601
Estimated Expiration: ⤷  Try a Trial

Patent: 19123736
Estimated Expiration: ⤷  Try a Trial

Mexico

Patent: 6727
Estimated Expiration: ⤷  Try a Trial

Patent: 14009528
Estimated Expiration: ⤷  Try a Trial

Spain

Patent: 50875
Estimated Expiration: ⤷  Try a Trial

Generics may enter earlier, or later, based on new patent filings, patent extensions, patent invalidation, early generic licensing, generic entry preferences, and other factors.

See the table below for additional patents covering QELBREE around the world.

Country Patent Number Title Estimated Expiration
Mexico 356727 FORMULACIONES DE LIBERACION MODIFICADA DE VILOXACINA. (MODIFIED RELEASE FORMULATIONS OF VILOXAZINE.) ⤷  Try a Trial
Canada 2864088 FORMULATIONS A LIBERATION MODIFIEE DE VILOXAZINE (MODIFIED RELEASE FORMULATIONS OF VILOXAZINE) ⤷  Try a Trial
Japan 2019123736 ビロキサジンの緩和放出製剤 (MODIFIED RELEASE FORMULATIONS OF VILOXAZINE) ⤷  Try a Trial
Canada 2735934 PROCEDE DE TRAITEMENT DE TROUBLE DEFICITAIRE DE L'ATTENTION AVEC HYPERACTIVITE (ADHD) (METHOD OF TREATMENT OF ATTENTION DEFICIT/HYPERACTIVITY DISORDER (ADHD)) ⤷  Try a Trial
>Country >Patent Number >Title >Estimated Expiration

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.