欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/H/0934/003
药品名称
CEFUROXIMA SANDOZ
活性成分
cefuroxime 500.0 mg
剂型
Film-coated tablet
上市许可持有人
Sandoz S.p.A Largo Umberto Boccioni 1 21040 - Origgio VA - Italy
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
Ireland (IE)
许可日期
2008/04/05
最近更新日期
2023/11/15
药物ATC编码
J01DA06 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
|
final common_outer_clean
Date of last change:2023/12/14
Final PL
|
final common_pl_clean
Date of last change:2023/11/15
Final SPC
|
final common_spc_clean
Date of last change:2023/11/15
Final Product Information
|
1_3_1 spc_label_pl _ common_outer _ cl
Date of last change:2021/01/08
Final Product Information
|
1_3_1 spc_label_pl _ common_pl _ cl
Date of last change:2021/01/08
Final Product Information
|
1_3_1 spc_label_pl _ common_spc _ cl
Date of last change:2021/01/08
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase