SULFISOXAZOLE Drug Patent Profile
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When do Sulfisoxazole patents expire, and what generic alternatives are available?
Sulfisoxazole is a drug marketed by Ani Pharms, Barr, Heather, Impax Labs, Lannett, Lederle, Pharmeral, Purepac Pharm, Rising, Roxane, Valeant Pharm Intl, Vitarine, Watson Labs, West Ward, and Sola Barnes Hind. and is included in fifteen NDAs.
The generic ingredient in SULFISOXAZOLE is sulfisoxazole diolamine. There are three drug master file entries for this compound. Additional details are available on the sulfisoxazole diolamine profile page.
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Summary for SULFISOXAZOLE
US Patents: | 0 |
Applicants: | 15 |
NDAs: | 15 |
Raw Ingredient (Bulk) Api Vendors: | 125 |
Clinical Trials: | 2 |
Patent Applications: | 4,359 |
DailyMed Link: | SULFISOXAZOLE at DailyMed |
Recent Clinical Trials for SULFISOXAZOLE
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Fundação de Amparo à Pesquisa do Estado de São Paulo | Phase 4 |
Federal University of São Paulo | Phase 4 |
University of Louisville | Early Phase 1 |
Medical Subject Heading (MeSH) Categories for SULFISOXAZOLE
US Patents and Regulatory Information for SULFISOXAZOLE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Ani Pharms | SULFISOXAZOLE | sulfisoxazole | TABLET;ORAL | 080142-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Pharmeral | SULFISOXAZOLE | sulfisoxazole | TABLET;ORAL | 084385-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Impax Labs | SULFISOXAZOLE | sulfisoxazole | TABLET;ORAL | 080109-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Vitarine | SULFISOXAZOLE | sulfisoxazole | TABLET;ORAL | 087332-001 | 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 |