BRETYLIUM TOSYLATE Drug Patent Profile
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When do Bretylium Tosylate patents expire, and what generic alternatives are available?
Bretylium Tosylate is a drug marketed by Abraxis Pharm, Astrazeneca, Breckenridge, Hikma, Hospira, Intl Medication, Luitpold, Abbott, B Braun, Baxter Hlthcare, and Hospira Inc. and is included in sixteen NDAs.
The generic ingredient in BRETYLIUM TOSYLATE is bretylium tosylate. There are three drug master file entries for this compound. Additional details are available on the bretylium tosylate profile page.
Summary for BRETYLIUM TOSYLATE
US Patents: | 0 |
Applicants: | 11 |
NDAs: | 16 |
Raw Ingredient (Bulk) Api Vendors: | 80 |
Patent Applications: | 1,359 |
DailyMed Link: | BRETYLIUM TOSYLATE at DailyMed |
Medical Subject Heading (MeSH) Categories for BRETYLIUM TOSYLATE
US Patents and Regulatory Information for BRETYLIUM TOSYLATE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Abraxis Pharm | BRETYLIUM TOSYLATE | bretylium tosylate | INJECTABLE;INJECTION | 070134-001 | Apr 29, 1986 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
B Braun | BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER | bretylium tosylate | INJECTABLE;INJECTION | 019121-003 | Apr 29, 1986 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Hikma | BRETYLIUM TOSYLATE | bretylium tosylate | INJECTABLE;INJECTION | 070545-001 | May 14, 1986 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Astrazeneca | BRETYLIUM TOSYLATE | bretylium tosylate | INJECTABLE;INJECTION | 071152-001 | Aug 10, 1987 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Luitpold | BRETYLIUM TOSYLATE | bretylium tosylate | INJECTABLE;INJECTION | 070891-001 | Jul 26, 1988 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |