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
Wyost Human denosumab denosumab EMEA/H/C/006378 Sandoz GmbH 2024/05/17 Authorised
Jubbonti Human denosumab denosumab EMEA/H/C/005964 Sandoz GmbH 2024/05/16 Authorised
Xgeva Human denosumab denosumab EMEA/H/C/002173 Amgen Europe B.V. 2011/07/13 Authorised
Prolia Human denosumab denosumab EMEA/H/C/001120 Amgen Europe B.V. 2010/05/26 Authorised
Stoboclo Human denosumab denosumab EMEA/H/C/006156 Celltrion Healthcare Hungary Kft. Opinion
Osenvelt Human denosumab denosumab EMEA/H/C/006157 Celltrion Healthcare Hungary Kft. Opinion
Obodence Human denosumab denosumab EMEA/H/C/006424 Samsung Bioepis NL B.V. Opinion
Xbryk Human denosumab denosumab EMEA/H/C/006468 Samsung Bioepis NL B.V. Opinion

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