PRUCALOPRIDE Drug Patent Profile
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When do Prucalopride patents expire, and what generic alternatives are available?
Prucalopride is a drug marketed by Ajanta Pharma Ltd, Alkem Labs Ltd, Amneal, Annora Pharma, Apotex, Appco, H2-pharma, Hikma, Lupin, MSN, Novitium Pharma, Somerset Therap, Specgx Llc, Teva Pharms Inc, Torrent, Zenara, and Zydus Lifesciences. and is included in seventeen NDAs.
The generic ingredient in PRUCALOPRIDE is prucalopride succinate. Seventeen suppliers are listed for this compound. Additional details are available on the prucalopride succinate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Prucalopride
A generic version of PRUCALOPRIDE was approved as prucalopride succinate by NOVITIUM PHARMA on December 26th, 2024.
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Questions you can ask:
- What is the 5 year forecast for PRUCALOPRIDE?
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Summary for PRUCALOPRIDE
| US Patents: | 0 |
| Applicants: | 17 |
| NDAs: | 17 |
| Drug Prices: | Drug price information for PRUCALOPRIDE |
| DailyMed Link: | PRUCALOPRIDE at DailyMed |
US Patents and Regulatory Information for PRUCALOPRIDE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Zenara | PRUCALOPRIDE SUCCINATE | prucalopride succinate | TABLET;ORAL | 218795-002 | Jun 24, 2025 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Teva Pharms Inc | PRUCALOPRIDE SUCCINATE | prucalopride succinate | TABLET;ORAL | 219071-002 | Feb 5, 2026 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Zydus Lifesciences | PRUCALOPRIDE SUCCINATE | prucalopride succinate | TABLET;ORAL | 218056-001 | Aug 7, 2025 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Torrent | PRUCALOPRIDE SUCCINATE | prucalopride succinate | TABLET;ORAL | 218778-001 | Jun 24, 2025 | DISCN | 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 |
