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
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
Neocolipor	Veterinary	Neonatal piglet colibacillosis vaccine (inactivated)	E. coli adhesin F4 (F4ab, F4ac, F4ad);E. coli adhesin F5;E. coli adhesin F6;E. coli adhesin F41	EMEA/V/C/000035	Boehringer Ingelheim Vetmedica GmbH	1998/04/14	Authorised
Clomicalm	Veterinary	Clomipramine	clomipramine hydrochloride	EMEA/V/C/000039	Virbac S.A.	1998/04/01	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
Primavax	Human	diphtheria, tetanus and hepatitis B (rDNA) vaccine (adsorbed)	Diphtheria toxoid;hepatitis B, recombinant surface antigen;tetanus toxoid	EMEA/H/C/000156	Pasteur Mà¨rieux MSD	1998/02/05	Withdrawn
Quadramet	Human	samarium [153Sm] lexidronam pentasodium	samarium (153Sm) lexidronam pentasodium	EMEA/H/C/000150	CIS bio international	1998/02/04	Authorised
Viramune	Human	nevirapine	nevirapine	EMEA/H/C/000183	Boehringer Ingelheim International GmbH	1998/02/04	Authorised
Viracept	Human	nelfinavir	nelfinavir	EMEA/H/C/000164	Roche Registration Ltd.	1998/01/22	Withdrawn
Dicural	Veterinary	difloxacin	difloxacin	EMEA/V/C/000031	Pfizer Limited	1998/01/16	Withdrawn
Quadrisol	Veterinary	vedaprofen	vedaprofen	EMEA/V/C/000032	VETCOOL B.V.	1997/12/04	Authorised
Cerezyme	Human	imiglucerase	imiglucerase	EMEA/H/C/000157	Sanofi B.V.	1997/11/17	Authorised
Daquiran	Human	pramipexole	pramipexole dihydrochloride monohydrate	EMEA/H/C/000135	Dr. Karl Thomae GmbH	1997/10/27	Withdrawn
Sifrol	Human	pramipexole	pramipexole dihydrochloride monohydrate	EMEA/H/C/000133	Boehringer Ingelheim International GmbH	1997/10/13	Authorised
BeneFIX	Human	nonacog alfa	Nonacog alfa	EMEA/H/C/000139	Pfizer Europe MA EEIG	1997/08/27	Authorised
Tasmar	Human	tolcapone	tolcapone	EMEA/H/C/000132	Viatris Healthcare Limited	1997/08/27	Authorised
Karvea	Human	irbesartan	irbesartan	EMEA/H/C/000142	Sanofi Winthrop Industrie	1997/08/26	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	-