TRICHLORMETHIAZIDE Drug Patent Profile
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Which patents cover Trichlormethiazide, and when can generic versions of Trichlormethiazide launch?
Trichlormethiazide is a drug marketed by Chartwell Rx, Impax Labs, Par Pharm, Sandoz, and Watson Labs. and is included in eleven NDAs.
The generic ingredient in TRICHLORMETHIAZIDE is reserpine; trichlormethiazide. There are nineteen drug master file entries for this compound. Additional details are available on the reserpine; trichlormethiazide profile page.
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Summary for TRICHLORMETHIAZIDE
| US Patents: | 0 |
| Applicants: | 5 |
| NDAs: | 11 |
| Raw Ingredient (Bulk) Api Vendors: | 84 |
| Patent Applications: | 4,049 |
| DailyMed Link: | TRICHLORMETHIAZIDE at DailyMed |
Medical Subject Heading (MeSH) Categories for TRICHLORMETHIAZIDE
Anatomical Therapeutic Chemical (ATC) Classes for TRICHLORMETHIAZIDE
US Patents and Regulatory Information for TRICHLORMETHIAZIDE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chartwell Rx | TRICHLORMETHIAZIDE | trichlormethiazide | TABLET;ORAL | 085568-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Watson Labs | TRICHLORMETHIAZIDE | trichlormethiazide | TABLET;ORAL | 086458-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Par Pharm | TRICHLORMETHIAZIDE | trichlormethiazide | TABLET;ORAL | 087005-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Watson Labs | TRICHLORMETHIAZIDE | trichlormethiazide | TABLET;ORAL | 083462-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Impax Labs | TRICHLORMETHIAZIDE | trichlormethiazide | TABLET;ORAL | 083967-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
