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Last Updated: April 27, 2024

MOEXIPRIL HYDROCHLORIDE Drug Patent Profile


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

Moexipril Hydrochloride is a drug marketed by Apotex Inc, Chartwell Rx, Glenmark Generics, Teva, Glenmark Pharms, and Heritage Pharms. and is included in eight NDAs.

The generic ingredient in MOEXIPRIL HYDROCHLORIDE is hydrochlorothiazide; moexipril hydrochloride. There are thirty-two drug master file entries for this compound. Additional details are available on the hydrochlorothiazide; moexipril hydrochloride profile page.

Drug patent expirations by year for MOEXIPRIL HYDROCHLORIDE
Recent Clinical Trials for MOEXIPRIL HYDROCHLORIDE

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SponsorPhase
University of NebraskaPhase 4
Teva Pharmaceuticals USAPhase 1
Mayo ClinicPhase 2

See all MOEXIPRIL HYDROCHLORIDE clinical trials

Pharmacology for MOEXIPRIL HYDROCHLORIDE
Anatomical Therapeutic Chemical (ATC) Classes for MOEXIPRIL HYDROCHLORIDE

US Patents and Regulatory Information for MOEXIPRIL HYDROCHLORIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Apotex Inc MOEXIPRIL HYDROCHLORIDE moexipril hydrochloride TABLET;ORAL 078454-001 Jun 2, 2008 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Teva MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE hydrochlorothiazide; moexipril hydrochloride TABLET;ORAL 076980-001 Mar 7, 2007 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Teva MOEXIPRIL HYDROCHLORIDE moexipril hydrochloride TABLET;ORAL 076204-001 May 8, 2003 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Chartwell Rx MOEXIPRIL HYDROCHLORIDE moexipril hydrochloride TABLET;ORAL 077536-002 Nov 30, 2006 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Glenmark Pharms MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE hydrochlorothiazide; moexipril hydrochloride TABLET;ORAL 090718-001 Mar 17, 2010 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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