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

MR编号	DK/H/0745/001
药品名称	Cefuroxim "Stragen"
活性成分	cefuroxime 250.0 mg
剂型	Powder for solution for injection
上市许可持有人	Stragen Nordic A/S Hesselvej 41 Ganløse 3660 Stenløse Denmark
参考成员国 - 产品名称	Denmark (DK)
互认成员国 - 产品名称	United Kingdom (Northern Ireland) (XI) Finland (FI)
许可日期	2005/04/19
最近更新日期	2024/01/12
药物ATC编码	J01DA06 Cefuroxime
申请类型	TypeLevel1：Abridged TypeLevel2：Initial Application TypeLevel3：Generic [Article 10.1.(a)(iii), first paragraph] TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final PL \| common_pl_cleanDate of last change:2023/08/10 Final SPC \| common_spc_cleanDate of last change:2023/08/10 Final Product Information \| DKH0745001-003IB015 Cefuroxim Stragen, IB variation common-outer-clean(1)Date of last change:2018/05/17 Final Product Information \| DKH0745001-003IB015 Cefuroxim Stragen, IB variation common-pl-cleanDate of last change:2018/05/17 Final Product Information \| DKH0745001-003IB015 Cefuroxim Stragen, IB variation common-outer-tracked (1)Date of last change:2018/05/17 Final Product Information \| DKH0745001-003IB015 Cefuroxim Stragen, IB variation common-spc-tracked (1)Date of last change:2018/05/17 Final Product Information \| DKH0745001-003IB015 Cefuroxim Stragen, IB variation common-pl-trackedDate of last change:2018/05/17 Final Product Information \| DKH0745001-003IB015 Cefuroxim Stragen, IB variation common-spc-clean (1)Date of last change:2018/05/17
市场状态	Positive