CLOMIPHENE Drug Patent Profile
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Which patents cover Clomiphene, and when can generic versions of Clomiphene launch?
Clomiphene is a drug marketed by Accord Hlthcare, Appco, Cosette, Novitium Pharma, and Rubicon. and is included in five NDAs.
The generic ingredient in CLOMIPHENE is clomiphene citrate. There are sixteen drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the clomiphene citrate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Clomiphene
A generic version of CLOMIPHENE was approved as clomiphene citrate by COSETTE on August 30th, 1999.
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Questions you can ask:
- What is the 5 year forecast for CLOMIPHENE?
- What are the global sales for CLOMIPHENE?
- What is Average Wholesale Price for CLOMIPHENE?
Summary for CLOMIPHENE
| US Patents: | 0 |
| Applicants: | 5 |
| NDAs: | 5 |
| Drug Prices: | Drug price information for CLOMIPHENE |
| DailyMed Link: | CLOMIPHENE at DailyMed |
US Patents and Regulatory Information for CLOMIPHENE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Accord Hlthcare | CLOMIPHENE CITRATE | clomiphene citrate | TABLET;ORAL | 219406-001 | Oct 3, 2025 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Novitium Pharma | CLOMIPHENE CITRATE | clomiphene citrate | TABLET;ORAL | 219781-001 | Oct 17, 2025 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Appco | CLOMIPHENE CITRATE | clomiphene citrate | TABLET;ORAL | 216739-001 | Nov 8, 2024 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Cosette | CLOMIPHENE CITRATE | clomiphene citrate | TABLET;ORAL | 075528-001 | Aug 30, 1999 | AB | RX | No | Yes | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Rubicon | CLOMIPHENE CITRATE | clomiphene citrate | TABLET;ORAL | 216545-001 | Nov 12, 2024 | 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 |
