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
Desloratadine ratiopharm	Human	desloratadine	desloratadine	EMEA/H/C/002404	Ratiopharm GmbH	2012/01/13	Authorised
Desloratadine Actavis	Human	desloratadine	desloratadine	EMEA/H/C/002435	Actavis Group PTC ehf	2012/01/13	Authorised
Dasselta	Human	desloratadine	desloratadine	EMEA/H/C/002310	Krka, d.d., Novo mesto	2011/11/28	Authorised
Desloratadine Teva	Human	desloratadine	desloratadine	EMEA/H/C/002419	Teva B.V	2011/11/24	Authorised
Aerinaze	Human	desloratadine, pseudoephedrine	desloratadine, pseudophedrine sulfate	EMEA/H/C/000772	N.V. Organon	2007/07/30	Authorised
Allex	Human	desloratadine	desloratadine	EMEA/H/C/000312	Schering-Plough Europe	2001/01/15	Withdrawn
Opulis	Human	desloratadine	desloratadine	EMEA/H/C/000311	Schering-Plough Europe	2001/01/15	Withdrawn
Neoclarityn	Human	desloratadine	desloratadine	EMEA/H/C/000314	N.V. Organon	2001/01/15	Authorised
Aerius	Human	desloratadine	desloratadine	EMEA/H/C/000313	N.V. Organon	2001/01/15	Authorised
Azomyr	Human	desloratadine	desloratadine	EMEA/H/C/000310	N.V. Organon	2001/01/15	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	-