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)
许可日期
2008/11/27
最近更新日期
2024/12/16
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 Labelling
|
common_outer_1500mg_nl4763_01_ib_016_trackchanges
Date of last change:2024/09/06
Final PL
|
Final PL
Date of last change:2024/09/06
Final SPC
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Final SmPC
Date of last change:2024/09/06
PubAR
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PAR 4763_Cefuroxim Fresenius 1500mg_20 February 2023
Date of last change:2024/09/06
PubAR Summary
|
sPAR 4762_Cefuroxim Fresenius 1500mg_ EN_20 February 2023
Date of last change:2024/09/06
Final Product Information
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DE912_Cefuroxim_pl_1500mg_trackchanges_post EORP_20131031_renewal
Date of last change:2024/09/06
Final Product Information
|
DE912_Cefuroxim_pl_750mg_trackchanges_post EORP_20131031_renewal
Date of last change:2024/09/06
Final Product Information
|
DE912_Cefuroxim_spc_1500mg_trackchanges_post EORP_20131031_renewal
Date of last change:2024/09/06
Final Product Information
|
DE912_Cefuroxim_spc_750mg_trackchanges__post EORP_20131031_renewal
Date of last change:2024/09/06
Final Product Information
|
DE913_Cefuroxim_pl_750mg_trackchanges_post EORP_20131031_renewal
Date of last change:2024/09/06
Final Product Information
|
DE913_Cefuroxim_spc_750mg_trackchanges_post EORP_20131031_renewal
Date of last change:2024/09/06
Final Product Information
|
DE914_Cefuroxim_common_pl_1500mg_trackchanges_post EORP_20131031_renewal
Date of last change:2024/09/06
Final Product Information
|
DE914_Cefuroxim_common_spc_1500mg_trackchanges_post EORP_20131031_renewal
Date of last change:2024/09/06
市场状态
Positive
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