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
Buccolam	Human	midazolam	midazolam	EMEA/H/C/002267	Neuraxpharm Pharmaceuticals S.L.	2011/09/04	Authorised
Votubia	Human	everolimus	everolimus	EMEA/H/C/002311	Novartis Europharm Limited	2011/09/02	Authorised
Vibativ	Human	telavancin	telavancin	EMEA/H/C/001240	Theravance Biopharma Ireland Umited	2011/09/02	Withdrawn
Levetiracetam ratiopharm	Human	levetiracetam	levetiracetam	EMEA/H/C/002244	ratiopharm GmbH	2011/08/26	Authorised
Levetiracetam Teva	Human	levetiracetam	levetiracetam	EMEA/H/C/002316	Teva B.V.	2011/08/25	Authorised
Trajenta	Human	linagliptin	linagliptin	EMEA/H/C/002110	Boehringer Ingelheim International GmbH	2011/08/23	Authorised
Levodopa/Carbidopa/Entacapone Orion	Human	levodopa;carbidopa;entacapone	levodopa;carbidopa;entacapone	EMEA/H/C/002441	Orion Corporation	2011/08/23	Authorised
Entacapone Orion	Human	entacapone	entacapone	EMEA/H/C/002440	Orion Corporation	2011/08/18	Authorised
Zulvac 1 Ovis	Veterinary	inactivated bluetongue virus, serotype-1	inactivated bluetongue virus, serotype-1	EMEA/V/C/002335	Zoetis Belgium SA	2011/08/05	Withdrawn
Zulvac 1 Bovis	Veterinary	inactivated bluetongue virus, serotype 1	inactivated bluetongue virus, serotype 1	EMEA/V/C/002334	Zoetis Belgium SA	2011/08/05	Withdrawn
Zoely	Human	nomegestrol;estradiol	nomegestrol acetate;estradiol	EMEA/H/C/001213	Theramex Ireland Limited	2011/07/26	Authorised
Ibandronic Acid Sandoz	Human	ibandronic acid	ibandronic acid	EMEA/H/C/002367	Sandoz GmbH	2011/07/26	Authorised
Tobi Podhaler	Human	tobramycin	tobramycin	EMEA/H/C/002155	Viatris Healthcare Limited	2011/07/20	Authorised
Fampyra	Human	fampridine	Fampridine	EMEA/H/C/002097	Merz Therapeutics GmbH	2011/07/20	Authorised
Victrelis	Human	boceprevir	Boceprevir	EMEA/H/C/002332	Merck Sharp Dohme Ltd	2011/07/18	Withdrawn
Yervoy	Human	ipilimumab	Ipilimumab	EMEA/H/C/002213	Bristol-Myers Squibb Pharma EEIG	2011/07/13	Authorised
Benlysta	Human	belimumab	belimumab	EMEA/H/C/002015	GlaxoSmithKline Trading Services Limited	2011/07/13	Authorised
Xgeva	Human	denosumab	denosumab	EMEA/H/C/002173	Amgen Europe B.V.	2011/07/13	Authorised
Temozolomide Sun	Human	temozolomide	temozolomide	EMEA/H/C/002198	Sun Pharmaceutical Industries Europe B.V.	2011/07/13	Authorised
Sprimeo HCT	Human	aliskiren;hydrochlorothiazide	aliskiren;hydrochlorothiazide	EMEA/H/C/002421	Novartis Europharm Ltd.	2011/06/23	Withdrawn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	-