欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	PT/H/1440/002
药品名称	Olmesartan + Hidroclorotiazida ratiopharm
活性成分	hydrochlorothiazide 25.0 mg olmesartan medoxomil 20.0 mg
剂型	Film-coated tablet
上市许可持有人	Teva Pharma - Produtos Farmacêuticos, Lda.
参考成员国 - 产品名称	Portugal (PT)
互认成员国 - 产品名称	Germany (DE) Olmesartan comp. AbZ 20 mg/25 mg Filmtabletten Italy (IT)
许可日期	2016/04/27
最近更新日期	2024/02/28
药物ATC编码	C09DA08 olmesartan medoxomil and diuretics
申请类型	TypeLevel1：Abridged TypeLevel2：Initial Application TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final Product Information \| common-labelling-20mgDate of last change:2016/06/21 Final Product Information \| common-labelling-40mgDate of last change:2016/06/21 Final Product Information \| common-pl-clean20mgDate of last change:2016/06/21 Final Product Information \| common-pl-clean40mgDate of last change:2016/06/21 Final Product Information \| common-spc-clean20mgDate of last change:2016/06/21 Final Product Information \| common-spc-clean40mgDate of last change:2016/06/21 PAR \| 598164_598163_598165_598162_20160609_PAR_IRSDate of last change:2016/06/21
市场状态	Positive