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
Duloxetine Zentiva	Human	duloxetine	duloxetine	EMEA/H/C/003935	Zentiva, k.s.	2015/08/20	Authorised
Duloxetine Viatris (previously Duloxetine Mylan)	Human	duloxetine	duloxetine	EMEA/H/C/003981	Mylan Pharmaceuticals Limited	2015/06/19	Authorised
Duloxetine Lilly	Human	duloxetine	duloxetine	EMEA/H/C/004000	Eli Lilly Nederland B.V.	2014/12/08	Authorised
Duloxetine Boehringer Ingelheim	Human	duloxetine	duloxetine	EMEA/H/C/001007	Boehringer Ingelheim International GmbH	2008/10/08	Withdrawn
Nodetrip (previously Xeristar)	Human	duloxetine	duloxetine	EMEA/H/C/000573	Esteve Pharmaceuticals, S.A.	2004/12/17	Withdrawn
Cymbalta	Human	duloxetine	duloxetine	EMEA/H/C/000572	Eli Lilly Nederland B.V.	2004/12/17	Authorised
Ariclaim	Human	duloxetine	duloxetine	EMEA/H/C/000552	Eli Lilly Nederland B.V.	2004/08/11	Withdrawn
Yentreve	Human	duloxetine	duloxetine hydrochloride	EMEA/H/C/000545	Eli Lilly Nederland B.V.	2004/08/11	Authorised
Duloxetine Sandoz	Human	duloxetine	duloxetine	EMEA/H/C/004009	Sandoz GmbH		Application withdrawn

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	-