欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/0913/001
药品名称
Cefuroxim Kabi 750 mg Pulver und Lösungsmittel zur Herstellung einer Infusionslösung
活性成分
cefuroxime 750.0 mg
剂型
Powder and solvent for solution for injection
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
Germany (DE)
互认成员国 - 产品名称
许可日期
2008/10/16
最近更新日期
2022/10/18
药物ATC编码
J01DC02 cefuroxime
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Multiple (Copy) Application
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Labelling
|
DE912_Cefuroxim_common_impack_1500mg_clean_20131010_renewal
Date of last change:2024/09/06
Final Labelling
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DE912_Cefuroxim_common_impack_750mg_clean_20131010_renewal
Date of last change:2024/09/06
Final Labelling
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DE912_Cefuroxim_common_outer_1500mg_clean_20131010_renewal
Date of last change:2024/09/06
Final Labelling
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DE912_Cefuroxim_common_outer_750mg_clean_20131010_renewal
Date of last change:2024/09/06
Final PL
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DE912_Cefuroxim_common_pl_1500mg_clean_20131010_renewal
Date of last change:2024/09/06
Final PL
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DE912_Cefuroxim_common_pl_750mg_clean_20131010_renewal
Date of last change:2024/09/06
Final SPC
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DE912_Cefuroxim_common_spc_1500mg_clean_20131010_renewal
Date of last change:2024/09/06
Final SPC
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DE912_Cefuroxim_common_spc_750mg_clean_20131010_renewal
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
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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 Labelling
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DE913_Cefuroxim_common_impack_750mg_clean_20131010_renewal
Date of last change:2024/09/06
Final Labelling
|
DE913_Cefuroxim_common_outer_750mg_clean_20131010_renewal
Date of last change:2024/09/06
Final PL
|
DE913_Cefuroxim_common_pl_750mg_clean_20131010_renewal
Date of last change:2024/09/06
Final SPC
|
DE913_Cefuroxim_common_spc_750mg_clean_20131010_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 Labelling
|
DE914_Cefuroxim_common_impack_1500mg_clean_20131010_renewal
Date of last change:2024/09/06
Final Labelling
|
DE914_Cefuroxim_common_outer_1500mg_clean_20131010_renewal
Date of last change:2024/09/06
Final PL
|
DE914_Cefuroxim_common_pl_1500mg_clean_20131010_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 SPC
|
DE914_Cefuroxim_common_spc_1500mg_clean_20131010_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
PubAR
|
PAREN_DE 0912_0914_Cefuroxime
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
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