欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
NL/H/4763/001
药品名称
Cefuroxim Kabi 1500 mg Pulver zur Herstellung einer Infusionslösung
活性成分
cefuroxime 1500.0 mg
剂型
Powder for solution for infusion
上市许可持有人
Fresenius Kabi Deutschland GmbH Else-Kröner-Str. 1 D-61352 Bad Homburg v.d.H.
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Belgium (BE)
France (FR)
许可日期
2008/11/27
最近更新日期
2023/08/01
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 PL
|
Final PL
Date of last change:2023/08/03
Final SPC
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Final SmPC
Date of last change:2023/08/03
PAR Summary
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sPAR 4762_Cefuroxim Fresenius 1500mg_ EN_20 February 2023
Date of last change:2023/02/20
PAR
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PAR 4763_Cefuroxim Fresenius 1500mg_20 February 2023
Date of last change:2023/02/20
Final Labelling
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common-outer-1500mg-nl4763_01-ib-016_trackchanges
Date of last change:2020/12/14
Final Product Information
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DE912_Cefuroxim_pl-750mg-trackchanges_post EORP_20131031_renewal
Date of last change:2013/10/31
Final Product Information
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DE912_Cefuroxim_pl-1500mg-trackchanges_post EORP_20131031_renewal
Date of last change:2013/10/31
Final Product Information
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DE912_Cefuroxim_spc-750mg-trackchanges__post EORP_20131031_renewal
Date of last change:2013/10/31
Final Product Information
|
DE912_Cefuroxim_spc-1500mg-trackchanges_post EORP_20131031_renewal
Date of last change:2013/10/31
Final Product Information
|
DE913_Cefuroxim_pl-750mg-trackchanges_post EORP_20131031_renewal
Date of last change:2013/10/31
Final Product Information
|
DE913_Cefuroxim_spc-750mg-trackchanges_post EORP_20131031_renewal
Date of last change:2013/10/31
Final Product Information
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DE914_Cefuroxim_common-pl-1500mg-trackchanges_post EORP_20131031_renewal
Date of last change:2013/10/31
Final Product Information
|
DE914_Cefuroxim_common-spc-1500mg-trackchanges_post EORP_20131031_renewal
Date of last change:2013/10/31
市场状态
Positive
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