欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/2773/007
药品名称
Lidolen
活性成分
lenalidomide 25.0 mg
剂型
Capsule, hard
上市许可持有人
Helm AG Nordkanalstrasse 28 20097 Hamburg Germany
参考成员国 - 产品名称
Denmark (DK)
Lidolen
互认成员国 - 产品名称
许可日期
2018/08/08
最近更新日期
2019/12/17
药物ATC编码
L04AX04 lenalidomide
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
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
Date of last change:2024/09/06
Final Labelling
|
common_outer
Date of last change:2024/09/06
Final PL
|
common_pl
Date of last change:2024/09/06
Final SPC
|
common_spc
Date of last change:2024/09/06
PubAR
|
PAR Lenalidomide DK_2773_001_007_DC
Date of last change:2024/09/06
PubAR Summary
|
summary PAR Lenalidomide DK_2773_001_007_DC
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
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European Union HMA Authorisation of Medicines DataBase