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Last Updated: March 29, 2024

FENOPROFEN CALCIUM Drug Patent Profile


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When do Fenoprofen Calcium patents expire, and when can generic versions of Fenoprofen Calcium launch?

Fenoprofen Calcium is a drug marketed by Am Therap, Halsey, Misemer, Par Pharm, Quantum Pharmics, Rising, Warner Chilcott, Watson Labs, Ani Pharms, Dava Pharms Inc, Ivax Sub Teva Pharms, Strides Pharma, Sun Pharm Industries, Usl Pharma, Watson Labs Teva, and Xspire Pharma. and is included in thirty-two NDAs.

The generic ingredient in FENOPROFEN CALCIUM is fenoprofen calcium. There are nine drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the fenoprofen calcium profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Fenoprofen Calcium

A generic version of FENOPROFEN CALCIUM was approved as fenoprofen calcium by XSPIRE PHARMA on August 17th, 1988.

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Summary for FENOPROFEN CALCIUM
Drug patent expirations by year for FENOPROFEN CALCIUM
Recent Clinical Trials for FENOPROFEN CALCIUM

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

SponsorPhase
Fundação de Amparo à Pesquisa do Estado de São PauloPhase 4
Federal University of São PauloPhase 4

See all FENOPROFEN CALCIUM clinical trials

Pharmacology for FENOPROFEN CALCIUM
Medical Subject Heading (MeSH) Categories for FENOPROFEN CALCIUM

US Patents and Regulatory Information for FENOPROFEN CALCIUM

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Watson Labs FENOPROFEN CALCIUM fenoprofen calcium TABLET;ORAL 072602-001 Oct 11, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Strides Pharma FENOPROFEN CALCIUM fenoprofen calcium TABLET;ORAL 072429-001 Aug 17, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs Teva FENOPROFEN CALCIUM fenoprofen calcium TABLET;ORAL 072407-001 Aug 17, 1988 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

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