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Last Updated: March 28, 2024

Amiloride hydrochloride; hydrochlorothiazide - Generic Drug Details


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What are the generic drug sources for amiloride hydrochloride; hydrochlorothiazide and what is the scope of patent protection?

Amiloride hydrochloride; hydrochlorothiazide is the generic ingredient in three branded drugs marketed by Barr, Chartwell Rx, Rising, Teva, Watson Labs, Par Pharm, and Merck, and is included in seven NDAs. Additional information is available in the individual branded drug profile pages.

Two suppliers are listed for this compound.

Summary for amiloride hydrochloride; hydrochlorothiazide
Recent Clinical Trials for amiloride hydrochloride; hydrochlorothiazide

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

SponsorPhase
Hospital de Clinicas de Porto AlegrePhase 3
Instituto de Cardiologia do Rio Grande do SulPhase 3
Guangdong Provincial People's HospitalPhase 4

See all amiloride hydrochloride; hydrochlorothiazide clinical trials

Pharmacology for amiloride hydrochloride; hydrochlorothiazide

US Patents and Regulatory Information for amiloride hydrochloride; hydrochlorothiazide

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Par Pharm HYDRO-RIDE amiloride hydrochloride; hydrochlorothiazide TABLET;ORAL 070347-001 Dec 25, 1990 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Rising AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE amiloride hydrochloride; hydrochlorothiazide TABLET;ORAL 073209-001 Oct 31, 1991 AB RX No Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Chartwell Rx AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE amiloride hydrochloride; hydrochlorothiazide TABLET;ORAL 073357-001 Nov 27, 1991 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE amiloride hydrochloride; hydrochlorothiazide TABLET;ORAL 073334-001 Jul 19, 1991 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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