ROPINIROLE Drug Patent Profile
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Which patents cover Ropinirole, and what generic alternatives are available?
Ropinirole is a drug marketed by Actavis Elizabeth, Alembic, Aurobindo Pharma Usa, Chartwell Rx, Dr Reddys Labs Ltd, Elite Labs Inc, Prinston Inc, Sandoz Inc, Watson Labs Inc, Accord Hlthcare, Alembic Ltd, Cosette, Epic Pharma Llc, Glenmark Pharms Ltd, Hikma, MLV, Orbion Pharms, Pharmobedient, and Zydus Lifesciences. and is included in twenty-one NDAs.
The generic ingredient in ROPINIROLE is ropinirole hydrochloride. There are fourteen drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the ropinirole hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Ropinirole
A generic version of ROPINIROLE was approved as ropinirole hydrochloride by PRINSTON INC on May 5th, 2008.
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Summary for ROPINIROLE
| US Patents: | 0 |
| Applicants: | 19 |
| NDAs: | 21 |
| Drug Prices: | Drug price information for ROPINIROLE |
| Drug Sales Revenues: | Drug sales revenues for ROPINIROLE |
| DailyMed Link: | ROPINIROLE at DailyMed |
US Patents and Regulatory Information for ROPINIROLE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Cosette | ROPINIROLE HYDROCHLORIDE | ropinirole hydrochloride | TABLET;ORAL | 077460-005 | May 5, 2008 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Mlv | ROPINIROLE HYDROCHLORIDE | ropinirole hydrochloride | TABLET;ORAL | 079165-006 | Feb 7, 2012 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Sandoz Inc | ROPINIROLE HYDROCHLORIDE | ropinirole hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 201047-006 | Jun 6, 2012 | AB | 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 |
