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
Amlodipine / Valsartan Mylan	Human	amlodipine;valsartan	amlodipine besilate;valsartan	EMEA/H/C/004037	Mylan Pharmaceuticals Limited	2016/03/22	Authorised
Onduarp	Human	telmisartan;amlodipine	telmisartan	EMEA/H/C/002118	Boehringer Ingelheim International GmbH	2011/11/24	Withdrawn
Rasitrio	Human	aliskiren;amlodipine;hydrochlorothiazide	aliskiren;amlodipine;hydrochlorothiazide	EMEA/H/C/002017	Novartis Europharm Ltd.	2011/11/22	Withdrawn
Rasilamlo	Human	aliskiren hemifumarate;amlodipine besilate	aliskiren;amlodipine	EMEA/H/C/002073	Novartis Europharm Ltd	2011/04/14	Withdrawn
Twynsta	Human	telmisartan;amlodipine	telmisartan;amlodipine	EMEA/H/C/001224	Boehringer Ingelheim International GmbH	2010/10/07	Authorised
Copalia HCT	Human	amlodipine;valsartan;hydrochlorothiazide	amlodipine;valsartan;hydrochlorothiazide	EMEA/H/C/001159	Novartis Europharm Limited	2009/11/03	Authorised
Dafiro HCT	Human	amlodipine besilate;valsartan;hydrochlorothiazide	valsartan;hydrochlorothiazide;amlodipine besilate	EMEA/H/C/001160	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
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amlodipine;valsartan	valsartan;amlodipine (as amlodipine besilate)	EMEA/H/C/000775	Novartis Europharm Ltd	2007/01/17	Withdrawn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
Lodipressin	Veterinary	amlodipine	amlodipine besilate	EMEA/V/C/003786	Le Vet Beheer B.V.		Refused

商品名称Name of medicine	*示例：Zokinvy（英文）
药品通用名或非专利名称International non-proprietary name (INN) / common name	*示例：lonafarnib（英文）
活性成分Active substance	*示例：lonafarnib（英文）
产品号EMA product number	*示例：EMEA/H/C/005271
ATC编号ATC code	*示例：L01EA06
上市许可开发者/申请人/持有人Marketing authorisation developer / applicant / holder	*示例：Janssen
药物治疗学分组Pharmacotherapeutic group	*示例：Antineoplastic
适应症Therapeutic indication	*示例：leukaemia
许可状态Medicine status
上市许可日期Marketing authorisation date	-