欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	AT/H/1393/002
药品名称	Cefuroxim Dr. Eberth 1500mg
活性成分	cefuroxime sodium salt 1500.0 mg
剂型	Powder for solution for injection/infusion
上市许可持有人	Dr Frederich Eberth Arzneimittel GmbH Am Bahnhof 2 Ursensollen, 92289
参考成员国 - 产品名称	Austria (AT) Cefuroxim Dr. Eberth 1500 mg Pulver zur Herstellung einer Injektions-/Infusionslösung
互认成员国 - 产品名称	Germany (DE) Cefuroxim Dr. Eberth 1500 mg Pulver zur Herstellung einer Injektions-/Infusionslösung
许可日期	2016/06/10
最近更新日期	2024/01/30
药物ATC编码	J01DC02 cefuroxime
申请类型	TypeLevel1：[not specified] TypeLevel2：[not specified] TypeLevel3：[not specified] TypeLevel4：[not specified] TypeLevel5：[not specified]
附件文件下载	Final SPC \| final_common_SmPC_AT_H_1393_001_002_IB_004_G_cleanDate of last change:2023/07/20 Final PL \| pil_common__1500mg_CLDate of last change:2023/07/20 PAR \| AT_H_1393_001_002_DC _ PARDate of last change:2023/05/15 Final Product Information \| MT_H_0195_001_LABDate of last change:2022/08/26 Final Product Information \| MT_H_0195_002_LABDate of last change:2022/08/26 Final Product Information \| MT_H_0195_001_002_SPCDate of last change:2022/08/26 Final Product Information \| MT_H_0195_001_PILDate of last change:2022/08/26 Final Product Information \| MT_H_0195_002_PILDate of last change:2022/08/26
市场状态	Positive