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	上市许可持有人/公司名称	上市批准日期	授权状态
Forcaltonin	Human	recombinant salmon calcitonin	Recombinant salmon calcitonin	EMEA/H/C/000197	Unigene UK Ltd.	1999/01/11	Withdrawn
Micardis	Human	telmisartan	Telmisartan	EMEA/H/C/000209	Boehringer Ingelheim International GmbH	1998/12/16	Authorised
Kinzalmono (previously Telmisartan Boehringer Ingelheim Pharma KG)	Human	telmisartan	Telmisartan	EMEA/H/C/000211	Bayer AG	1998/12/16	Authorised
Pritor	Human	telmisartan	Telmisartan	EMEA/H/C/000210	Bayer AG	1998/12/11	Authorised
Prometax	Human	rivastigmine	rivastigmine	EMEA/H/C/000255	Novartis Europharm Limited	1998/12/03	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
Simulect	Human	basiliximab	basiliximab	EMEA/H/C/000207	Novartis Europharm Limited	1998/10/09	Authorised
HumaSPECT	Human	votumumab	votumumab	EMEA/H/C/000145	KS Biomedix Limited	1998/09/25	Withdrawn
Comtan	Human	entacapone	entacapone	EMEA/H/C/000171	Orion Corporation	1998/09/22	Authorised
Zartra	Human	imiquimod	imiquimod	EMEA/H/C/000180	Laboratoires 3M Santé	1998/09/18	Withdrawn
Aldara	Human	imiquimod	imiquimod	EMEA/H/C/000179	Viatris Healthcare Limited	1998/09/18	Authorised
Comtess	Human	entacapone	entacapone	EMEA/H/C/000170	Orion Corporation	1998/09/16	Authorised
Patrex	Human	sildenafil	sildenafil	EMEA/H/C/000204	Pfizer Limited	1998/09/15	Withdrawn
Viagra	Human	sildenafil	sildenafil	EMEA/H/C/000202	Upjohn EESV	1998/09/13	Authorised
Fortovase	Human	saquinavir	saquinavir	EMEA/H/C/000178	Roche Registration Ltd.	1998/08/20	Withdrawn
NovoNorm	Human	repaglinide	repaglinide	EMEA/H/C/000187	Novo Nordisk A/S	1998/08/16	Authorised
Suvaxyn Aujeszky 783 + O/W	Veterinary	live attenuated Aujeszky's disease virus	live attenuated Aujeszky's disease virus	EMEA/V/C/000038	Zoetis Belgium SA	1998/08/07	Authorised
Optruma	Human	raloxifene	raloxifene hydrochloride	EMEA/H/C/000185	Eli Lilly Nederland B.V.	1998/08/05	Authorised
Evista	Human	raloxifene	raloxifene hydrochloride	EMEA/H/C/000184	Substipharm	1998/08/05	Authorised

药品名称Medicine name	*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Product number	*示例：EMEA/H/C/005271
ATC编号ATC code	*示例：L01EA06
上市许可持有人/公司名称Marketing authorisation holder/company name	*示例：Janssen
人用药物治疗分组Human pharmacotherapeutic group	*示例：Antineoplastic
适应症Condition / indication	*示例：leukaemia
授权状态Authorisation status
上市批准日期Marketing authorisation date	-