欧盟EMA药品数据库-欧盟集中审批药品
(European Medicines Agency Authorisation of Medicines DataBase)
商品名称 适用类别 通用名称 活性成分 产品号 上市许可开发者/申请人/持有人 上市许可日期 许可状态
Rasitrio Human aliskiren;amlodipine;hydrochlorothiazide aliskiren;amlodipine;hydrochlorothiazide EMEA/H/C/002017 Novartis Europharm Ltd. 2011/11/22 Withdrawn
Sprimeo HCT Human aliskiren;hydrochlorothiazide aliskiren;hydrochlorothiazide EMEA/H/C/002421 Novartis Europharm Ltd. 2011/06/23 Withdrawn
Rasilamlo Human aliskiren hemifumarate;amlodipine besilate aliskiren;amlodipine EMEA/H/C/002073 Novartis Europharm Ltd 2011/04/14 Withdrawn
Riprazo HCT Human aliskiren;hydrochlorothiazide aliskiren;hydrochlorothiazide EMEA/H/C/002420 Novartis Europharm Ltd. 2011/04/13 Withdrawn
Rasilez HCT Human aliskiren;hydrochlorothiazide aliskiren;hydrochlorothiazide EMEA/H/C/000964 Noden Pharma DAC 2009/01/16 Withdrawn
Rasilez Human aliskiren aliskiren EMEA/H/C/000780 Noden Pharma DAC 2007/08/22 Authorised
Riprazo Human aliskiren aliskiren EMEA/H/C/000853 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Sprimeo Human aliskiren aliskiren EMEA/H/C/000851 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Enviage Human aliskiren aliskiren EMEA/H/C/000850 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Tekturna Human aliskiren aliskiren EMEA/H/C/000852 Novartis Europharm Ltd. 2007/08/22 Withdrawn

数据库说明:

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