欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/4371/001
药品名称
Cefuroxim Mylan 250mg
活性成分
Cefuroxime axetil 250.0 mg
剂型
Film-coated tablet
上市许可持有人
Mylan
参考成员国 - 产品名称
Netherlands (NL)
Cefuroxim Mylan 250 mg, filmomhulde tabletten
互认成员国 - 产品名称
Italy (IT)
许可日期
2019/06/26
最近更新日期
2024/11/22
药物ATC编码
J01DC02 cefuroxime
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial 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
PubAR
|
190823 NL_H_4371_001_002_DC Cefuroxim Mylan PAR
Date of last change:2024/09/06
PubAR Summary
|
190823 NL_H_4371_001_002_DC Cefuroxim Mylan summary EN
Date of last change:2024/09/06
Final PL
|
common_pl_nl4371_v008_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_nl4371_v008_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase