ROCURONIUM Drug Patent Profile
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When do Rocuronium patents expire, and when can generic versions of Rocuronium launch?
Rocuronium is a drug marketed by Aspiro, Caplin, Eugia Pharma, Fresenius Kabi Usa, Gland, Hikma, Hospira, Knack, Mankind Pharma, Meitheal, Mylan Institutional, Piramal Critical, Prinston Inc, Rising, Sagent Pharms Inc, Sandoz, Shandong, Steriscience, Tamarang, Teva Pharms, West Ward Pharm Corp, and B Braun Medical. and is included in twenty-three NDAs. There is one patent protecting this drug.
The generic ingredient in ROCURONIUM is rocuronium bromide. There are eleven drug master file entries for this compound. Twenty-six suppliers are listed for this compound. Additional details are available on the rocuronium bromide profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Rocuronium
A generic version of ROCURONIUM was approved as rocuronium bromide by HOSPIRA on November 26th, 2008.
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Summary for ROCURONIUM
| US Patents: | 0 |
| Applicants: | 22 |
| NDAs: | 23 |
| Drug Prices: | Drug price information for ROCURONIUM |
| What excipients (inactive ingredients) are in ROCURONIUM? | ROCURONIUM excipients list |
| DailyMed Link: | ROCURONIUM at DailyMed |
US Patents and Regulatory Information for ROCURONIUM
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| B Braun Medical | ROCURONIUM BROMIDE | rocuronium bromide | SOLUTION;INTRAVENOUS | 219108-001 | Oct 24, 2025 | RX | Yes | Yes | 11,998,605 | ⤷ Start Trial | Y | ⤷ Start Trial | |||
| Shandong | ROCURONIUM BROMIDE | rocuronium bromide | INJECTABLE;INJECTION | 215684-001 | Jul 12, 2024 | AP | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Sagent Pharms Inc | ROCURONIUM BROMIDE | rocuronium bromide | INJECTABLE;INJECTION | 091458-001 | Jul 28, 2010 | AP | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |


