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Last Updated: March 28, 2024

PROGESTERONE Drug Patent Profile


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

Progesterone is a drug marketed by Amneal Pharms Ny, Bionpharma, Dr Reddys, Eugia Pharma, Sofgen Pharms, Teva Pharms, Xiromed, Accord Hlthcare, Actavis Labs Ut Inc, Am Regent, Fresenius Kabi Usa, Hikma Farmaceutica, and Lilly. and is included in fifteen NDAs.

The generic ingredient in PROGESTERONE is progesterone. There are fifty-seven drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the progesterone profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Progesterone

A generic version of PROGESTERONE was approved as progesterone by FRESENIUS KABI USA on April 25th, 2001.

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Drug patent expirations by year for PROGESTERONE
Drug Prices for PROGESTERONE

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Drug Sales Revenue Trends for PROGESTERONE

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Recent Clinical Trials for PROGESTERONE

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SponsorPhase
Fayoum UniversityN/A
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)Phase 4
Fundación Santiago Dexeus FontPhase 3

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Pharmacology for PROGESTERONE
Drug ClassProgesterone
Medical Subject Heading (MeSH) Categories for PROGESTERONE

US Patents and Regulatory Information for PROGESTERONE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Amneal Pharms Ny PROGESTERONE progesterone CAPSULE;ORAL 207724-001 Sep 7, 2017 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Eugia Pharma PROGESTERONE progesterone INJECTABLE;INJECTION 210965-001 Dec 6, 2018 AO RX No Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Eugia Pharma PROGESTERONE progesterone CAPSULE;ORAL 211285-001 Oct 26, 2018 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Bionpharma PROGESTERONE progesterone CAPSULE;ORAL 200900-002 Aug 16, 2013 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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