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Last Updated: April 26, 2024

OFORTA Drug Patent Profile


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

Oforta is a drug marketed by Sanofi Aventis Us and is included in one NDA.

The generic ingredient in OFORTA is fludarabine phosphate. There are ten drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the fludarabine phosphate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Oforta

A generic version of OFORTA was approved as fludarabine phosphate by HIKMA on August 28th, 2003.

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Drug patent expirations by year for OFORTA
Recent Clinical Trials for OFORTA

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Jonsson Comprehensive Cancer CenterPhase 1
Bristol-Myers SquibbPhase 1
Stand Up To CancerPhase 1

See all OFORTA clinical trials

US Patents and Regulatory Information for OFORTA

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Sanofi Aventis Us OFORTA fludarabine phosphate TABLET;ORAL 022273-001 Dec 18, 2008 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  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

Expired US Patents for OFORTA

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Sanofi Aventis Us OFORTA fludarabine phosphate TABLET;ORAL 022273-001 Dec 18, 2008 ⤷  Try a Trial ⤷  Try a Trial
Sanofi Aventis Us OFORTA fludarabine phosphate TABLET;ORAL 022273-001 Dec 18, 2008 ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

International Patents for OFORTA

See the table below for patents covering OFORTA around the world.

Country Patent Number Title Estimated Expiration
Japan 2009040797 METHOD FOR PRODUCTION OF FLUDARABINE-PHOSPHATE LITHIUM, SODIUM, POTASSIUM, CALCIUM AND MAGNESIUM SALTS, PURIFICATION METHOD FOR PRODUCING FLUDARABINE PHOSPHATE AND FLUDARABINE PHOSPHATE HAVING PURITY OF AT LEAST 99.5% ⤷  Try a Trial
Germany 29825173 ⤷  Try a Trial
New Zealand 533701 Ultrapure oral fludara formulation with a fast releasing active substance ⤷  Try a Trial
Slovakia 8872000 PURIFICATION METHOD FOR PRODUCING FLUDARABIN PHOSPHATE ⤷  Try a Trial
Germany 59807096 ⤷  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.