ACCURETIC Drug Patent Profile
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When do Accuretic patents expire, and what generic alternatives are available?
Accuretic is a drug marketed by Pfizer Pharms and is included in one NDA.
The generic ingredient in ACCURETIC is hydrochlorothiazide; quinapril hydrochloride. There are thirty-two drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; quinapril hydrochloride profile page.
Summary for ACCURETIC
US Patents: | 0 |
Applicants: | 1 |
NDAs: | 1 |
Finished Product Suppliers / Packagers: | 2 |
Raw Ingredient (Bulk) Api Vendors: | 128 |
Clinical Trials: | 3 |
Patent Applications: | 3,370 |
Formulation / Manufacturing: | see details |
Drug Prices: | Drug price information for ACCURETIC |
What excipients (inactive ingredients) are in ACCURETIC? | ACCURETIC excipients list |
DailyMed Link: | ACCURETIC at DailyMed |
Recent Clinical Trials for ACCURETIC
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Ranbaxy Laboratories Limited | N/A |
Mylan Pharmaceuticals | Phase 1 |
Pharmacology for ACCURETIC
Drug Class | Angiotensin Converting Enzyme Inhibitor Thiazide Diuretic |
Mechanism of Action | Angiotensin-converting Enzyme Inhibitors |
Physiological Effect | Increased Diuresis |
Anatomical Therapeutic Chemical (ATC) Classes for ACCURETIC
US Patents and Regulatory Information for ACCURETIC
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-001 | Dec 28, 1999 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-002 | Dec 28, 1999 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-003 | Dec 28, 1999 | DISCN | Yes | 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 |
Expired US Patents for ACCURETIC
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
---|---|---|---|---|---|---|---|
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-001 | Dec 28, 1999 | ⤷ Try a Trial | ⤷ Try a Trial |
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-003 | Dec 28, 1999 | ⤷ Try a Trial | ⤷ Try a Trial |
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-001 | Dec 28, 1999 | ⤷ Try a Trial | ⤷ Try a Trial |
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-003 | Dec 28, 1999 | ⤷ Try a Trial | ⤷ Try a Trial |
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-002 | Dec 28, 1999 | ⤷ Try a Trial | ⤷ Try a Trial |
Pfizer Pharms | ACCURETIC | hydrochlorothiazide; quinapril hydrochloride | TABLET;ORAL | 020125-002 | Dec 28, 1999 | ⤷ Try a Trial | ⤷ Try a Trial |
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
International Patents for ACCURETIC
See the table below for patents covering ACCURETIC around the world.
Country | Patent Number | Title | Estimated Expiration |
---|---|---|---|
Germany | 3176029 | ⤷ Try a Trial | |
Hungary | 183602 | PROCESS FOR PRODUCING 1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID'S SUBSTITUTED ACYL DERIVATIVES | ⤷ Try a Trial |
Finland | 79839 | ⤷ Try a Trial | |
German Democratic Republic | 201787 | VERFAHREN ZUR HERSTELLUNG VON SUBSTITUIERTEN ACYLDERIVATEN VON 1,2,3,4-TETRAHYDROISOCHINOLIN-3-CARBONSAEUREN | ⤷ Try a Trial |
Japan | S5788164 | SUBSTITUTED ACYL DERIVATIVE OF 1,2,3,4- TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID | ⤷ Try a Trial |
New Zealand | 223407 | STABILISED ACE INHIBITOR COMPOSITIONS | ⤷ Try a Trial |
Norway | 159017 | ⤷ Try a Trial | |
>Country | >Patent Number | >Title | >Estimated Expiration |
Supplementary Protection Certificates for ACCURETIC
Patent Number | Supplementary Protection Certificate | SPC Country | SPC Expiration | SPC Description |
---|---|---|---|---|
0480717 | 98C0025 | Belgium | ⤷ Try a Trial | PRODUCT NAME: LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE; NAT. REGISTRATION NO/DATE: NL 20 037 19950215; FIRST REGISTRATION: FR - NL 20 037 19950215 |
0049605 | SPC/GB93/099 | United Kingdom | ⤷ Try a Trial | SPC/GB93/099, EXPIRES: 20040413 |
0454511 | 99C0009 | Belgium | ⤷ Try a Trial | PRODUCT NAME: IRBESARTAN / HYDROCHLOROTHIAZIDE; REGISTRATION NO/DATE: EU/1/98/086/001 19981015 |
0503785 | CA 2011 00026 | Denmark | ⤷ Try a Trial | PRODUCT NAME: A COMBINATION OF OLMESARTAN MEDOXOMIL, OPTIONALLY IN THE FORM OF A PHARMACEUTICALLY ACCEPTABLE SALT, AND AMLODIPINE BESYLATE AND HYDROCHLOROTHIAZIDE; NAT. REG. NO/DATE: 46260-46269 (DK) 20110323; FIRST REG. NO/DATE: DE 79810.00.00 20101216 |
0565634 | 06C0030 | France | ⤷ Try a Trial | PRODUCT NAME: EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE; NAT. REGISTRATION NO/DATE: NL 32075 20060623; FIRST REGISTRATION: LI - 55783 01 20020607 |
0502314 | SPC/GB02/037 | United Kingdom | ⤷ Try a Trial | PRODUCT NAME: TELMISARTAN, OPTIONALLY IN THE FORM OF A PHARMACEUTICALLY ACCEPTABLE SALT, AND HYDROCHLOROTHIAZIDE; REGISTERED: UK EU/1/02/213/001 20020419; UK EU/1/02/213/002 20020419; UK EU/1/02/213/003 20020419; UK EU/1/02/214/004 20020419; UK EU/1/02/213/005 20020419; UK EU/1/02/213/006 20020419; UK EU/1/02/213/007 20020419; UK EU/1/02/213/008 20020419; UK EU/1/02/213/009 20020419; UK EU/1/02/213/010 20020419 |
0096157 | SPC/GB95/011 | United Kingdom | ⤷ Try a Trial | SPC/GB95/011:, EXPIRES: 20060930 |
>Patent Number | >Supplementary Protection Certificate | >SPC Country | >SPC Expiration | >SPC Description |