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
Cymbalta	Human	duloxetine	duloxetine	EMEA/H/C/000572	Eli Lilly Nederland B.V.	2004/12/17	Authorised
Nodetrip (previously Xeristar)	Human	duloxetine	duloxetine	EMEA/H/C/000573	Esteve Pharmaceuticals, S.A.	2004/12/17	Withdrawn
Kivexa	Human	abacavir, lamivudine	abacavir, lamivudine	EMEA/H/C/000581	ViiV Healthcare BV	2004/12/16	Authorised
Xagrid	Human	anagrelide	Anagrelide	EMEA/H/C/000480	Takeda Pharmaceuticals International AG Ireland Branch	2004/11/15	Authorised
Mimpara	Human	cinacalcet	cinacalcet hydrochloride	EMEA/H/C/000570	Amgen Europe B.V.	2004/10/22	Authorised
Emselex	Human	darifenacin hydrobromide	darifenacin hydrobromide	EMEA/H/C/000554	pharmaand GmbH	2004/10/22	Authorised
Parareg	Human	cinacalcet	cinacalcet	EMEA/H/C/000575	Dompé Biotec S.p.A.	2004/10/22	Withdrawn
Wilzin	Human	zinc	zinc	EMEA/H/C/000535	Recordati Rare Diseases	2004/10/12	Authorised
Apidra	Human	insulin glulisine	insulin glulisine	EMEA/H/C/000557	sanofi-aventis Deutschland GmbH	2004/09/27	Authorised
Alimta	Human	pemetrexed	pemetrexed	EMEA/H/C/000564	Eli Lilly Nederland B.V.	2004/09/20	Authorised
Osseor	Human	strontium ranelate	strontium ranelate	EMEA/H/C/000561	Les Laboratoires Servier	2004/09/20	Withdrawn
Protelos	Human	strontium ranelate	strontium ranelate	EMEA/H/C/000560	Les Laboratoires Servier	2004/09/20	Withdrawn
Angiox	Human	bivalirudin	Bivalirudin	EMEA/H/C/000562	The Medicines Company UK Ltd	2004/09/20	Withdrawn
Raptiva	Human	efalizumab	efalizumab	EMEA/H/C/000542	Serono Europe Limited	2004/09/20	Withdrawn
Previcox	Veterinary	firocoxib	firocoxib	EMEA/V/C/000082	Boehringer Ingelheim Vetmedica GmbH	2004/09/13	Authorised
Aivlosin	Veterinary	tylvalosin	tylvalosin	EMEA/V/C/000083	ECO Animal Health Europe Limited	2004/09/09	Authorised
Nobivac Piro	Veterinary	vaccine against babesiosis in dogs	babesia canis, inactivated, babesia rossi, inactivated	EMEA/V/C/000084	Intervet International BV	2004/09/02	Withdrawn
Yentreve	Human	duloxetine	duloxetine hydrochloride	EMEA/H/C/000545	Eli Lilly Nederland B.V.	2004/08/11	Authorised
Ariclaim	Human	duloxetine	duloxetine	EMEA/H/C/000552	Eli Lilly Nederland B.V.	2004/08/11	Withdrawn
Pedea	Human	ibuprofen	Ibuprofen	EMEA/H/C/000549	Recordati Rare Diseases	2004/07/28	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	-