TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE) - Generic Drug Details
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What are the generic drug sources for triple sulfa (sulfabenzamide;sulfacetamide;sulfathiazole) and what is the scope of freedom to operate?
Triple sulfa (sulfabenzamide;sulfacetamide;sulfathiazole)
is the generic ingredient in five branded drugs marketed by Cosette, Ortho Mcneil Pharm, Alpharma Us Pharms, Fougera, Padagis Us, Savage Labs, and Pharmaderm, and is included in nine NDAs. Additional information is available in the individual branded drug profile pages.Summary for TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
US Patents: | 0 |
Tradenames: | 5 |
Applicants: | 7 |
NDAs: | 9 |
Raw Ingredient (Bulk) Api Vendors: | 6 |
Patent Applications: | 137 |
DailyMed Link: | TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE) at DailyMed |
Anatomical Therapeutic Chemical (ATC) Classes for TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
US Patents and Regulatory Information for TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Fougera | TRIPLE SULFA | triple sulfa (sulfabenzamide;sulfacetamide;sulfathiazole) | CREAM;VAGINAL | 086424-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Fougera | TRIPLE SULFA | triple sulfa (sulfabenzamide;sulfacetamide;sulfathiazole) | TABLET;VAGINAL | 088463-001 | Jan 3, 1985 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Savage Labs | TRYSUL | triple sulfa (sulfabenzamide;sulfacetamide;sulfathiazole) | CREAM;VAGINAL | 087887-001 | Jul 23, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Ortho Mcneil Pharm | SULTRIN | triple sulfa (sulfabenzamide;sulfacetamide;sulfathiazole) | CREAM;VAGINAL | 005794-001 | 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 |