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Last Updated: March 29, 2024

MECLOFENAMATE SODIUM Drug Patent Profile


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Which patents cover Meclofenamate Sodium, and when can generic versions of Meclofenamate Sodium launch?

Meclofenamate Sodium is a drug marketed by Am Therap, Ani Pharms, Barr, Chartwell Rx, Mylan, Par Pharm, Usl Pharma, Vitarine, and Watson Labs. and is included in eighteen NDAs.

The generic ingredient in MECLOFENAMATE SODIUM is meclofenamate sodium. There are eight drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the meclofenamate sodium profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Meclofenamate Sodium

A generic version of MECLOFENAMATE SODIUM was approved as meclofenamate sodium by MYLAN on September 3rd, 1986.

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Drug patent expirations by year for MECLOFENAMATE SODIUM
Recent Clinical Trials for MECLOFENAMATE SODIUM

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

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US Patents and Regulatory Information for MECLOFENAMATE SODIUM

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Am Therap MECLOFENAMATE SODIUM meclofenamate sodium CAPSULE;ORAL 071362-001 Feb 10, 1987 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs MECLOFENAMATE SODIUM meclofenamate sodium CAPSULE;ORAL 071640-001 Aug 11, 1987 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Chartwell Rx MECLOFENAMATE SODIUM meclofenamate sodium CAPSULE;ORAL 072262-001 Nov 29, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Ani Pharms MECLOFENAMATE SODIUM meclofenamate sodium CAPSULE;ORAL 071469-001 Apr 15, 1987 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Par Pharm MECLOFENAMATE SODIUM meclofenamate sodium CAPSULE;ORAL 072078-001 Mar 10, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs MECLOFENAMATE SODIUM meclofenamate sodium CAPSULE;ORAL 071641-001 Aug 11, 1987 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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