Last Updated: October 2, 2026

Doxecitine; doxribtimine - Generic Drug Details


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What are the generic drug sources for doxecitine; doxribtimine and what is the scope of patent protection?

Doxecitine; doxribtimine is the generic ingredient in one branded drug marketed by Ucb Inc and is included in one NDA. There are two patents protecting this compound. Additional information is available in the individual branded drug profile pages.

One supplier is listed for this compound.

Summary for doxecitine; doxribtimine
International Patents:64
US Patents:2
Tradenames:1
Applicants:1
NDAs:1
Finished Product Suppliers / Packagers: 1
DailyMed Link:doxecitine; doxribtimine at DailyMed
DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for doxecitine; doxribtimine
Generic Entry Date for doxecitine; doxribtimine*:
Constraining patent/regulatory exclusivity:

NEW CHEMICAL ENTITY

Dosage:

FOR SOLUTION;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.

US Patents and Regulatory Information for doxecitine; doxribtimine

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Ucb Inc KYGEVVI doxecitine; doxribtimine FOR SOLUTION;ORAL 219792-001 Nov 3, 2025 RX Yes Yes 10,471,087 ⤷  Start Trial ⤷  Start Trial
Ucb Inc KYGEVVI doxecitine; doxribtimine FOR SOLUTION;ORAL 219792-001 Nov 3, 2025 RX Yes Yes ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Ucb Inc KYGEVVI doxecitine; doxribtimine FOR SOLUTION;ORAL 219792-001 Nov 3, 2025 RX Yes Yes 11,649,259 ⤷  Start Trial Y ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Supplementary Protection Certificates for doxecitine; doxribtimine

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
3310362 301385 Netherlands ⤷  Start Trial PRODUCT NAME: DOXECITINE EN DOXRIBTIMINE; REGISTRATION NO/DATE: EU/1/25/2013 20260327
3310362 CR 2026 00027 Denmark ⤷  Start Trial PRODUCT NAME: DOXECITIN OG DOXRIBTIMIN; REG. NO/DATE: EU/1/25/2013 20260327
3310362 C20265012 Finland ⤷  Start Trial
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description

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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. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. 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.