欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Clopidogrel TAD
适用类别Human
治疗领域Peripheral Vascular Diseases;Stroke;Myocardial Infarction
通用名/非专利名称clopidogrel
活性成分clopidogrel (as hydrochloride)
产品号EMEA/H/C/001136
患者安全信息No
许可状态Authorised
ATC编码B01AC04
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2009/09/23
上市许可开发者/申请人/持有人Tad Pharma GmbH
人用药物治疗学分组Antithrombotic agents
兽用药物治疗学分组
审评意见日期2009/06/25
欧盟委员会决定日期2025/05/13
修订号17
治疗适应症Clopidogrel is indicated in adults for the prevention of atherothrombotic events in: Patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease.
适用物种
兽用药物ATC编码
首次发布日期2018/05/10
最后更新日期2025/05/13
产品说明书https://www.ema.europa.eu/en/documents/product-information/clopidogrel-tad-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/clopidogrel-tad
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase