欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Esmya
适用类别Human
治疗领域Leiomyoma
通用名/非专利名称ulipristal
活性成分ulipristal acetate
产品号EMEA/H/C/002041
患者安全信息No
许可状态Withdrawn
ATC编码G03XB02
是否额外监管No
是否仿制药或hybrid药物No
是否生物类似药No
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2012/02/22
上市许可开发者/申请人/持有人Gedeon Richter Ltd 
人用药物治疗学分组Sex hormones and modulators of the genital system
兽用药物治疗学分组
审评意见日期2011/12/15
欧盟委员会决定日期2021/01/11
修订号16
治疗适应症Ulipristal acetate is indicated for pre-operative treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age. Ulipristal acetate is indicated for intermittent treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age.
适用物种
兽用药物ATC编码
首次发布日期2018/07/26
最后更新日期2025/08/20
产品说明书https://www.ema.europa.eu/en/documents/product-information/esmya-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/esmya
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