Treatment: Method for providing post coital contraception to a woman by administering about 30 mg of ulipristal acetate within about 120 hours after intercourse, wherein the woman is overweight having a bmi of ...
| Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
|---|---|---|---|---|
| These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
| US8962603 | LAB HRA PHARMA | Method for post coital contraception in overweight or obese female subjects using ulipristal acetate |
Jun, 2030
(4 years from now) | |
| US8426392 | LAB HRA PHARMA | Method for providing emergency contraception |
Jun, 2030
(4 years from now) | |
| US9283233 | LAB HRA PHARMA | Method for on-demand contraception |
Apr, 2030
(4 years from now) | |
| US10159681 | LAB HRA PHARMA | Method for on-demand contraception |
Apr, 2030
(4 years from now) | |
| US10772897 | LAB HRA PHARMA | Method for on-demand contraception |
Apr, 2030
(4 years from now) | |
| US8735380 | LAB HRA PHARMA | Ulipristal acetate tablets |
Feb, 2029
(3 years from now) | |
| US9844510 | LAB HRA PHARMA | Ulipristal acetate tablets |
Dec, 2028
(2 years from now) | |
| US8512745 | LAB HRA PHARMA | Ulipristal acetate tablets |
Jun, 2030
(4 years from now) | |
| Drug Exclusivity | Drug Exclusivity Expiration |
|---|---|
| New Chemical Entity Exclusivity(NCE) | Aug 13, 2015 |
| M(M-271) | Jun 24, 2024 |
Drugs and Companies using ULIPRISTAL ACETATE ingredient
NCE-1 date: 13 August, 2014
Market Authorisation Date: 13 August, 2010
Dosage: TABLET