欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0618/001
药品名称
Cefudoc
活性成分
cefuroxime 250.0 mg
剂型
Film-coated tablet
上市许可持有人
Aristo Pharma GmbH Wallenroder Strasse 8 - 10 13435 Berlin Germany
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Portugal (PT)
Poland (PL)
Zamur 250 mg
许可日期
2004/06/15
最近更新日期
2024/04/02
药物ATC编码
J01DA06 Cefuroxime
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic Article 4.8(a)(iii), first paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
common_pl_cefuroxime_250mg_500mg_fct_V13_0423_cl
Date of last change:2023/09/14
Final SPC
|
common_smpc_cefuroxime_250mg_500mg_fct_V04_0423_cl
Date of last change:2023/09/14
Final Labelling
|
common-labop-cefu-250mg-clean
Date of last change:2021/01/22
Final Product Information
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common-spc-250-500mg_08-2016_track_changes
Date of last change:2016/12/19
Final Product Information
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common-outer-250mg_08-2016_f
Date of last change:2016/12/19
Final Product Information
|
common-outer-500mg_08-2016_f
Date of last change:2016/12/19
Final Product Information
|
common-outer-250mg_08-2016_track_changes
Date of last change:2016/12/19
Final Product Information
|
common-pl-250mg_08-2016_f
Date of last change:2016/12/19
Final Product Information
|
common-outer-500mg_08-2016_track_changes
Date of last change:2016/12/19
Final Product Information
|
common-pl-500mg_08-2016_track_changes
Date of last change:2016/12/19
Final Product Information
|
common-pl-250mg_08-2016_track_changes
Date of last change:2016/12/19
Final Product Information
|
common-pl-500mg_08-2016_f
Date of last change:2016/12/19
Final Product Information
|
common-spc-250-500mg_08-2016_f
Date of last change:2016/12/19
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase