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
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Allex Human desloratadine desloratadine EMEA/H/C/000312 Schering-Plough Europe 2001/01/15 Withdrawn
Opulis Human desloratadine desloratadine EMEA/H/C/000311 Schering-Plough Europe 2001/01/15 Withdrawn
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
Neoclarityn Human desloratadine desloratadine EMEA/H/C/000314 N.V. Organon 2001/01/15 Authorised
Desloratadine Krka Human desloratadine desloratadine EMEA/H/C/002461 Krka, d.d., Novo mesto Application withdrawn

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