FLECAINIDE Drug Patent Profile
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When do Flecainide patents expire, and what generic alternatives are available?
Flecainide is a drug marketed by Amneal Pharm, Ani Pharms, Aurobindo Pharma Ltd, Chartwell, Hikma, Omsav Pharma, Regcon Holdings, Sun Pharm Inds Ltd, and Yichang Humanwell. and is included in ten NDAs.
The generic ingredient in FLECAINIDE is flecainide acetate. There are ten drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the flecainide acetate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Flecainide
A generic version of FLECAINIDE was approved as flecainide acetate by AMNEAL PHARM on July 31st, 2001.
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Questions you can ask:
- What is the 5 year forecast for FLECAINIDE?
- What are the global sales for FLECAINIDE?
- What is Average Wholesale Price for FLECAINIDE?
Summary for FLECAINIDE
| US Patents: | 0 |
| Applicants: | 9 |
| NDAs: | 10 |
| Drug Prices: | Drug price information for FLECAINIDE |
| Drug Sales Revenues: | Drug sales revenues for FLECAINIDE |
| DailyMed Link: | FLECAINIDE at DailyMed |
US Patents and Regulatory Information for FLECAINIDE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Yichang Humanwell | FLECAINIDE ACETATE | flecainide acetate | TABLET;ORAL | 215599-001 | Sep 8, 2022 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Yichang Humanwell | FLECAINIDE ACETATE | flecainide acetate | TABLET;ORAL | 215599-002 | Sep 8, 2022 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Amneal Pharm | FLECAINIDE ACETATE | flecainide acetate | TABLET;ORAL | 075442-001 | Jul 31, 2001 | 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 |



