欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NO/H/0320/001
药品名称
Cefalexin Antibiotice
活性成分
cefalexin monohydrate 500.0 mg
剂型
Capsule, hard
上市许可持有人
Antibiotice SA 1 Valea Lupului Street Iasi 707410 Romania
参考成员国 - 产品名称
Norway (NO)
互认成员国 - 产品名称
Finland (FI)
许可日期
2022/01/20
最近更新日期
2020/06/25
药物ATC编码
J01DB01 cefalexin
申请类型
TypeLevel1:
Known Active Substance
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
Final Labelling
|
common_impack_EOP
Date of last change:2024/09/06
Final Labelling
|
common_outer_EOP
Date of last change:2024/09/06
Final PL
|
common_pl_EOP
Date of last change:2024/09/06
Final SPC
|
common_spc_EOP
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase