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
ViraferonPeg	Human	peginterferon alfa-2b	peginterferon alfa-2b	EMEA/H/C/000329	Merck Sharp Dohme Ltd	2000/05/28	Withdrawn
PegIntron	Human	peginterferon alfa-2b	peginterferon alfa-2b	EMEA/H/C/000280	Merck Sharp & Dohme B.V.	2000/05/24	Withdrawn
Orgalutran	Human	ganirelix	ganirelix	EMEA/H/C/000274	Organon N.V.	2000/05/16	Authorised
Azopt	Human	brinzolamide	brinzolamide	EMEA/H/C/000267	Novartis Europharm Limited	2000/03/09	Authorised
Thyrogen	Human	thyrotropin alfa	thyrotropin alfa	EMEA/H/C/000220	Sanofi B.V.	2000/03/09	Authorised
IntronA	Human	interferon alfa-2b	interferon alfa-2b	EMEA/H/C/000281	Merck Sharp & Dohme B.V.	2000/03/09	Withdrawn
Bovalto Ibraxion	Veterinary	infectious bovine rhinotracheitis vaccine (inactivated)	inactivated IBR virus	EMEA/V/C/000051	Merial	2000/03/09	Withdrawn
Viraferon	Human	interferon alfa-2b	interferon alfa-2b	EMEA/H/C/000282	Schering-Plough Europe	2000/03/09	Withdrawn
Zyprexa Velotab	Human	olanzapine	olanzapine	EMEA/H/C/000287	CHEPLAPHARM Registration GmbH	2000/02/03	Authorised
Enbrel	Human	etanercept	etanercept	EMEA/H/C/000262	Pfizer Europe MA EEIG	2000/02/02	Authorised
Renagel	Human	sevelamer	sevelamer	EMEA/H/C/000254	Sanofi Winthrop Industrie	2000/01/28	Authorised
Tractocile	Human	atosiban	atosiban (as acetate)	EMEA/H/C/000253	Ferring Pharmaceuticals A/S	2000/01/20	Authorised
Ammonaps	Human	sodium phenylbutyrate	sodium phenylbutyrate	EMEA/H/C/000219	Immedica Pharma AB	1999/12/07	Authorised
Tikosyn	Human	dofetilide	dofetilide	EMEA/H/C/000238	Pfizer Limited	1999/11/29	Withdrawn
Doxirobe	Veterinary	doxycycline	doxycycline	EMEA/V/C/000044	Pfizer Limited	1999/09/16	Withdrawn
NovoRapid	Human	insulin aspart	insulin aspart	EMEA/H/C/000258	Novo Nordisk A/S	1999/09/07	Authorised
Arava	Human	leflunomide	leflunomide	EMEA/H/C/000235	Sanofi-aventis Deutschland GmbH	1999/09/02	Authorised
Ferriprox	Human	deferiprone	Deferiprone	EMEA/H/C/000236	Chiesi Farmaceutici S.p.A.	1999/08/25	Authorised
Remicade	Human	infliximab	infliximab	EMEA/H/C/000240	Janssen Cilag International NV	1999/08/13	Authorised
Synagis	Human	palivizumab	palivizumab	EMEA/H/C/000257	AstraZeneca AB	1999/08/13	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	-