欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0618/002
药品名称
Cefudoc
活性成分
cefuroxime 500.0 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 500 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 Labelling
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common_labop_cefu_250mg_clean
Date of last change:2024/09/06
Final Product Information
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common_outer_250mg_08_2016_f
Date of last change:2024/09/06
Final Product Information
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common_outer_250mg_08_2016_track_changes
Date of last change:2024/09/06
Final Product Information
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common_outer_500mg_08_2016_f
Date of last change:2024/09/06
Final Product Information
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common_outer_500mg_08_2016_track_changes
Date of last change:2024/09/06
Final Product Information
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common_pl_250mg_08_2016_f
Date of last change:2024/09/06
Final Product Information
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common_pl_250mg_08_2016_track_changes
Date of last change:2024/09/06
Final Product Information
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common_pl_500mg_08_2016_f
Date of last change:2024/09/06
Final Product Information
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common_pl_500mg_08_2016_track_changes
Date of last change:2024/09/06
Final PL
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common_pl_cefuroxime_250mg_500mg_fct_V13_0423_cl
Date of last change:2024/09/06
Final SPC
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common_smpc_cefuroxime_250mg_500mg_fct_V04_0423_cl
Date of last change:2024/09/06
Final Product Information
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common_spc_250_500mg_08_2016_f
Date of last change:2024/09/06
Final Product Information
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common_spc_250_500mg_08_2016_track_changes
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase