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Last Updated: March 28, 2024

GEMFIBROZIL Drug Patent Profile


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Which patents cover Gemfibrozil, and what generic alternatives are available?

Gemfibrozil is a drug marketed by Mylan, Purepac Pharm, Apotex, Ascent Pharms Inc, Aurobindo Pharma Ltd, Cadila, Cadila Pharms Ltd, Caribe Holdings, Chartwell Molecules, Chartwell Rx, Hikma Pharms, Impax Pharms, Invagen Pharms, Northstar Hlthcare, Sun Pharm Inds Inc, Teva, and Watson Labs. and is included in twenty NDAs.

The generic ingredient in GEMFIBROZIL is gemfibrozil. Thirty-three suppliers are listed for this compound. Additional details are available on the gemfibrozil profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Gemfibrozil

A generic version of GEMFIBROZIL was approved as gemfibrozil by CHARTWELL MOLECULES on September 27th, 1993.

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Drug patent expirations by year for GEMFIBROZIL
Drug Prices for GEMFIBROZIL

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Drug Sales Revenue Trends for GEMFIBROZIL

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Recent Clinical Trials for GEMFIBROZIL

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SponsorPhase
St. Louis UniversityEarly Phase 1
Polaryx Therapeutics, Inc.Phase 3
Bristol-Myers SquibbPhase 1

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Medical Subject Heading (MeSH) Categories for GEMFIBROZIL
Anatomical Therapeutic Chemical (ATC) Classes for GEMFIBROZIL

US Patents and Regulatory Information for GEMFIBROZIL

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Mylan GEMFIBROZIL gemfibrozil CAPSULE;ORAL 073466-001 Jan 25, 1993 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Teva GEMFIBROZIL gemfibrozil TABLET;ORAL 074256-001 Oct 31, 1993 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Cadila Pharms Ltd GEMFIBROZIL gemfibrozil TABLET;ORAL 203266-001 Jun 17, 2016 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Ascent Pharms Inc GEMFIBROZIL gemfibrozil TABLET;ORAL 214603-001 Jan 13, 2021 AB RX 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

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