欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Teriflunomide Accord
适用类别Human
治疗领域Multiple Sclerosis, Relapsing-Remitting
通用名/非专利名称teriflunomide
活性成分teriflunomide
产品号EMEA/H/C/005960
患者安全信息No
许可状态Authorised
ATC编码L04AA31
是否额外监管No
是否仿制药或hybrid药物Yes
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2022/11/09
上市许可开发者/申请人/持有人Accord Healthcare S.L.U.
人用药物治疗学分组Immunosuppressants;Selective immunosuppressants
兽用药物治疗学分组
审评意见日期2022/09/15
欧盟委员会决定日期2024/07/26
修订号3
治疗适应症Teriflunomide Accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (MS) (please refer to section 5.1 for important information on the population for which efficacy has been established).
适用物种
兽用药物ATC编码
首次发布日期2022/09/14
最后更新日期2024/07/29
产品说明书https://www.ema.europa.eu/en/documents/product-information/teriflunomide-accord-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/teriflunomide-accord
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