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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检索条件：VALSARTAN
数据记录共 11 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 上市许可持有人/公司名称 上市批准日期 授权状态
Neparvis Human sacubitril, valsartan sacubitril, valsartan EMEA/H/C/004343 Novartis Europharm Limited 2016/05/26 Authorised
Amlodipine / Valsartan Mylan Human amlodipine, valsartan Amlodipine besilate, valsartan EMEA/H/C/004037 Mylan Pharmaceuticals Limited 2016/03/22 Authorised
Entresto Human sacubitril, valsartan sacubitril, valsartan EMEA/H/C/004062 Novartis Europharm Limited 2015/11/19 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hydrochlorothiazide amlodipine, valsartan, hydrochlorothiazide EMEA/H/C/001161 Novartis Europharm Ltd. 2009/10/15 Withdrawn
Imprida Human amlodipine, valsartan valsartan, amlodipine (as amlodipine besilate) EMEA/H/C/000775 Novartis Europharm Ltd 2007/01/17 Withdrawn
Exforge Human amlodipine, valsartan valsartan, amlodipine (as amlodipine besilate) EMEA/H/C/000716 Novartis Europharm Limited 2007/01/16 Authorised
Dafiro Human amlodipine, valsartan amlodipine, valsartan EMEA/H/C/000776 Novartis Europharm Limited 2007/01/15 Authorised
Copalia Human amlodipine, valsartan valsartan, amlodipine (as amlodipine besilate) EMEA/H/C/000774 Novartis Europharm Limited 2007/01/15 Authorised

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