Hydrochlorothiazide; propranolol hydrochloride - Generic Drug Details
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What are the generic drug sources for hydrochlorothiazide; propranolol hydrochloride and what is the scope of freedom to operate?
Hydrochlorothiazide; propranolol hydrochloride
is the generic ingredient in seven branded drugs marketed by Wyeth Ayerst, Wyeth Pharms Inc, Duramed Pharms Barr, Actavis Elizabeth, Ani Pharms, Chartwell Rx, Ivax Sub Teva Pharms, Rising, Warner Chilcott, and Watson Labs, and is included in nineteen NDAs. Additional information is available in the individual branded drug profile pages.Summary for hydrochlorothiazide; propranolol hydrochloride
US Patents: | 0 |
Tradenames: | 7 |
Applicants: | 10 |
NDAs: | 19 |
Raw Ingredient (Bulk) Api Vendors: | 1 |
Clinical Trials: | 1 |
DailyMed Link: | hydrochlorothiazide; propranolol hydrochloride at DailyMed |
Recent Clinical Trials for hydrochlorothiazide; propranolol hydrochloride
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
VA Office of Research and Development | |
US Department of Veterans Affairs |
See all hydrochlorothiazide; propranolol hydrochloride clinical trials
Anatomical Therapeutic Chemical (ATC) Classes for hydrochlorothiazide; propranolol hydrochloride
US Patents and Regulatory Information for hydrochlorothiazide; propranolol hydrochloride
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Watson Labs | PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | hydrochlorothiazide; propranolol hydrochloride | TABLET;ORAL | 070301-001 | Apr 18, 1986 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Rising | PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | hydrochlorothiazide; propranolol hydrochloride | TABLET;ORAL | 070947-002 | Mar 4, 1987 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Ani Pharms | PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | hydrochlorothiazide; propranolol hydrochloride | TABLET;ORAL | 072043-001 | Mar 14, 1988 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Wyeth Pharms Inc | INDERIDE-80/25 | hydrochlorothiazide; propranolol hydrochloride | TABLET;ORAL | 018031-002 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Wyeth Pharms Inc | INDERIDE-40/25 | hydrochlorothiazide; propranolol hydrochloride | TABLET;ORAL | 018031-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Ani Pharms | PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | hydrochlorothiazide; propranolol hydrochloride | TABLET;ORAL | 070705-002 | Oct 1, 1986 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Duramed Pharms Barr | PROPRANOLOL HYDROCHLORIDE & HYDROCHLOROTHIAZIDE | hydrochlorothiazide; propranolol hydrochloride | TABLET;ORAL | 071126-001 | Mar 2, 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 |
Expired US Patents for hydrochlorothiazide; propranolol hydrochloride
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
---|---|---|---|---|---|---|---|
Wyeth Ayerst | INDERIDE LA 80/50 | hydrochlorothiazide; propranolol hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 019059-001 | Jul 3, 1985 | ⤷ Try a Trial | ⤷ Try a Trial |
Wyeth Ayerst | INDERIDE LA 120/50 | hydrochlorothiazide; propranolol hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 019059-002 | Jul 3, 1985 | ⤷ Try a Trial | ⤷ Try a Trial |
Wyeth Ayerst | INDERIDE LA 160/50 | hydrochlorothiazide; propranolol hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 019059-003 | Jul 3, 1985 | ⤷ Try a Trial | ⤷ Try a Trial |
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |