HYDROXYPROGESTERONE Drug Patent Profile
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Which patents cover Hydroxyprogesterone, and what generic alternatives are available?
Hydroxyprogesterone is a drug marketed by Allergan, Epic Pharma Llc, Aspen Global Inc, and Eugia Pharma. and is included in four NDAs.
The generic ingredient in HYDROXYPROGESTERONE is hydroxyprogesterone caproate. There are twelve drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the hydroxyprogesterone caproate profile page.
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Summary for HYDROXYPROGESTERONE
| US Patents: | 0 |
| Applicants: | 4 |
| NDAs: | 4 |
| Drug Prices: | Drug price information for HYDROXYPROGESTERONE |
| DailyMed Link: | HYDROXYPROGESTERONE at DailyMed |
US Patents and Regulatory Information for HYDROXYPROGESTERONE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Allergan | HYDROXYPROGESTERONE CAPROATE | hydroxyprogesterone caproate | INJECTABLE;INJECTION | 017439-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Aspen Global Inc | HYDROXYPROGESTERONE CAPROATE | hydroxyprogesterone caproate | SOLUTION;INTRAMUSCULAR | 200271-001 | Aug 24, 2015 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Allergan | HYDROXYPROGESTERONE CAPROATE | hydroxyprogesterone caproate | INJECTABLE;INJECTION | 017439-002 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Epic Pharma Llc | HYDROXYPROGESTERONE CAPROATE | hydroxyprogesterone caproate | INJECTABLE;INJECTION | 018004-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Eugia Pharma | HYDROXYPROGESTERONE CAPROATE | hydroxyprogesterone caproate | SOLUTION;INTRAMUSCULAR | 211142-001 | May 9, 2019 | 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 |
