欧盟EMA药品数据库-欧盟集中审批药品
（European Medicines Agency Authorisation of Medicines DataBase）
请输入需要查询的英文药品名称，通用名称，活性成分，产品号
*Search by Medicine name,INN,Active substance,Product number.
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数据记录共 19 条，共 1 页，当前第 1 页
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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
Tolucombi Human telmisartan;hydrochlorothiazide telmisartan;hydrochlorothiazide EMEA/H/C/002549 Krka, d.d., Novo mesto 2013/03/13 Authorised
Actelsar HCT Human telmisartan;hydrochlorothiazide telmisartan;hydrochlorothiazide EMEA/H/C/002676 Actavis Group PTC ehf 2013/03/13 Authorised
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aliskiren;amlodipine;hydrochlorothiazide EMEA/H/C/002017 Novartis Europharm Ltd. 2011/11/22 Withdrawn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Human aliskiren;hydrochlorothiazide aliskiren;hydrochlorothiazide EMEA/H/C/002421 Novartis Europharm Ltd. 2011/06/23 Withdrawn
Riprazo HCT Human aliskiren;hydrochlorothiazide aliskiren;hydrochlorothiazide EMEA/H/C/002420 Novartis Europharm Ltd. 2011/04/13 Withdrawn
Ifirmacombi Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/002302 Krka, d.d., Novo mesto 2011/03/04 Authorised
Irbesartan/Hydrochlorothiazide Teva Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/001112 Teva B.V.  2009/11/26 Authorised
Dafiro HCT Human amlodipine besilate;valsartan;hydrochlorothiazide valsartan;hydrochlorothiazide;amlodipine besilate EMEA/H/C/001160 Novartis Europharm Limited 2009/11/03 Authorised
Copalia HCT Human amlodipine;valsartan;hydrochlorothiazide amlodipine;valsartan;hydrochlorothiazide EMEA/H/C/001159 Novartis Europharm Limited 2009/11/03 Authorised
Exforge HCT Human amlodipine besilate;valsartan;hydrochlorothiazide valsartan;hydrochlorothiazide;amlodipine besilate EMEA/H/C/001068 Novartis Europharm Limited 2009/10/15 Authorised
Imprida HCT Human amlodipine;valsartan;hydrochlorothiazide amlodipine;valsartan;hydrochlorothiazide EMEA/H/C/001161 Novartis Europharm Ltd. 2009/10/15 Lapsed
Rasilez HCT Human aliskiren;hydrochlorothiazide aliskiren;hydrochlorothiazide EMEA/H/C/000964 Noden Pharma DAC 2009/01/16 Withdrawn
Irbesartan Hydrochlorothiazide BMS Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/000784 Bristol-Myers Squibb Pharma EEIG 2007/01/19 Withdrawn
Irbesartan Hydrochlorothiazide Zentiva (previously Irbesartan Hydrochlorothiazide Winthrop) Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/000783 sanofi-aventis groupe  2007/01/18 Authorised
PritorPlus Human telmisartan;hydrochlorothiazide telmisartan;hydrochlorothiazide EMEA/H/C/000414 Bayer AG 2002/04/22 Authorised
MicardisPlus Human telmisartan;hydrochlorothiazide EMEA/H/C/000413 Boehringer Ingelheim International GmbH 2002/04/19 Authorised
Kinzalkomb Human telmisartan;hydrochlorothiazide telmisartan;hydrochlorothiazide EMEA/H/C/000415 Bayer AG 2002/04/19 Authorised
Karvezide Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/000221 Sanofi Winthrop Industrie 1998/10/16 Authorised
CoAprovel Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/000222 Sanofi Winthrop Industrie 1998/10/14 Authorised

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