PHENYLBUTAZONE Drug Patent Profile
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Which patents cover Phenylbutazone, and what generic alternatives are available?
Phenylbutazone is a drug marketed by Chartwell Rx, Ivax Pharms, Sun Pharm Industries, Watson Labs, and Fosun Pharma. and is included in eight NDAs.
The generic ingredient in PHENYLBUTAZONE is phenylbutazone. There are nine drug master file entries for this compound. Additional details are available on the phenylbutazone profile page.
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Summary for PHENYLBUTAZONE
US Patents: | 0 |
Applicants: | 5 |
NDAs: | 8 |
Raw Ingredient (Bulk) Api Vendors: | 118 |
Clinical Trials: | 1 |
Patent Applications: | 3,791 |
DailyMed Link: | PHENYLBUTAZONE at DailyMed |
Recent Clinical Trials for PHENYLBUTAZONE
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Federal University of São Paulo | Phase 4 |
Fundação de Amparo à Pesquisa do Estado de São Paulo | Phase 4 |
Medical Subject Heading (MeSH) Categories for PHENYLBUTAZONE
Anatomical Therapeutic Chemical (ATC) Classes for PHENYLBUTAZONE
US Patents and Regulatory Information for PHENYLBUTAZONE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Chartwell Rx | PHENYLBUTAZONE | phenylbutazone | CAPSULE;ORAL | 087774-001 | Jun 16, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Watson Labs | PHENYLBUTAZONE | phenylbutazone | TABLET;ORAL | 086151-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Watson Labs | PHENYLBUTAZONE | phenylbutazone | CAPSULE;ORAL | 087756-001 | Dec 17, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Watson Labs | PHENYLBUTAZONE | phenylbutazone | TABLET;ORAL | 087674-001 | Apr 21, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Ivax Pharms | PHENYLBUTAZONE | phenylbutazone | CAPSULE;ORAL | 088218-001 | Jun 24, 1983 | 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 |