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
Fortovase	Human	saquinavir	saquinavir	EMEA/H/C/000178	Roche Registration Ltd.	1998/08/20	Withdrawn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
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
Xenical	Human	orlistat	orlistat	EMEA/H/C/000154	CHEPLAPHARM Arzneimittel GmbH	1998/07/29	Authorised
EchoGen	Human	dodecafluoropentane	dodecafluoropentane	EMEA/H/C/000149	Sonus Pharmaceuticals Ltd.	1998/07/17	Withdrawn
Plavix	Human	clopidogrel	clopidogrel hydrogen sulfate	EMEA/H/C/000174	Sanofi Winthrop Industrie	1998/07/15	Authorised
Iscover	Human	clopidogrel	clopidogrel	EMEA/H/C/000175	Sanofi Winthrop Industrie	1998/07/14	Authorised
Turvel	Human	trovafloxacin	trovafloxacin	EMEA/H/C/000158	Pfizer Limited	1998/07/08	Withdrawn
Turvel IV	Human	trovafloxacin	alatrofloxacin mesilate	EMEA/H/C/000159	Pfizer Limited	1998/07/03	Withdrawn
Trovan IV	Human	trovafloxacin	alatrofloxacin mesilate	EMEA/H/C/000161	Pfizer Limited	1998/07/03	Withdrawn
Trovan	Human	trovafloxacin	trovafloxacin	EMEA/H/C/000160	Pfizer Limited	1998/07/03	Withdrawn
Pylori-Chek	Human	13C-urea	urea (13C)	EMEA/H/C/000182	Alimenterics B.V.	1998/06/15	Withdrawn
MabThera	Human	rituximab	rituximab	EMEA/H/C/000165	Roche Registration GmbH	1998/06/02	Authorised
Optison	Human	perflutren	perflutren	EMEA/H/C/000166	GE Healthcare AS	1998/05/17	Authorised
Exelon	Human	rivastigmine	rivastigmine	EMEA/H/C/000169	Novartis Europharm Limited	1998/05/11	Authorised
Pylobactell	Human	13C-urea	urea (13C)	EMEA/H/C/000151	Richen Europe S.R.L	1998/05/07	Authorised
Rebif	Human	interferon beta-1a	interferon beta-1a	EMEA/H/C/000136	Merck Europe B.V.	1998/05/03	Authorised
Combivir	Human	lamivudine;zidovudine	lamivudine;zidovudine	EMEA/H/C/000190	ViiV Healthcare BV	1998/03/18	Authorised
Mirapexin	Human	pramipexole	pramipexole dihydrochloride monohydrate	EMEA/H/C/000134	Boehringer Ingelheim International GmbH	1998/02/23	Authorised

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	-