CHLORPROPAMIDE Drug Patent Profile
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When do Chlorpropamide patents expire, and when can generic versions of Chlorpropamide launch?
Chlorpropamide is a drug marketed by Ani Pharms, Dava Pharms Inc, Halsey, Norvium Bioscience, Par Pharm, Rising, Sandoz, Superpharm, Usl Pharma, Watson Labs, and Watson Labs Teva. and is included in thirty-one NDAs.
The generic ingredient in CHLORPROPAMIDE is chlorpropamide. There are eleven drug master file entries for this compound. Additional details are available on the chlorpropamide profile page.
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Questions you can ask:
- What is the 5 year forecast for CHLORPROPAMIDE?
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- What is Average Wholesale Price for CHLORPROPAMIDE?
Summary for CHLORPROPAMIDE
| US Patents: | 0 |
| Applicants: | 11 |
| NDAs: | 31 |
| Raw Ingredient (Bulk) Api Vendors: | 112 |
| Clinical Trials: | 5 |
| Patent Applications: | 3,553 |
| DailyMed Link: | CHLORPROPAMIDE at DailyMed |
Recent Clinical Trials for CHLORPROPAMIDE
Identify potential brand extensions & 505(b)(2) entrants
| Sponsor | Phase |
|---|---|
| Canadian Institutes of Health Research (CIHR) | |
| Canadian Network for Observational Drug Effect Studies, CNODES | |
| Drug Safety and Effectiveness Network, Canada |
Medical Subject Heading (MeSH) Categories for CHLORPROPAMIDE
Anatomical Therapeutic Chemical (ATC) Classes for CHLORPROPAMIDE
US Patents and Regulatory Information for CHLORPROPAMIDE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Watson Labs Teva | CHLORPROPAMIDE | chlorpropamide | TABLET;ORAL | 088852-001 | Sep 26, 1984 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Watson Labs | CHLORPROPAMIDE | chlorpropamide | TABLET;ORAL | 086865-001 | Sep 24, 1984 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Watson Labs | CHLORPROPAMIDE | chlorpropamide | TABLET;ORAL | 088608-001 | Apr 12, 1984 | 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 |
