欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0347/001
药品名称
Symla
活性成分
lamotrigine 25.0 mg
剂型
Tablet
上市许可持有人
Former RMS: PT/H/1123/001 Symphar Sp. Z o. o.
参考成员国 - 产品名称
Poland (PL)
Symla
互认成员国 - 产品名称
许可日期
2014/02/21
最近更新日期
2020/03/02
药物ATC编码
N03AX09 lamotrigine
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
|
common_outer_track 06_19
Date of last change:2024/09/06
Final PL
|
common_pl_track 06_19
Date of last change:2024/09/06
Final SPC
|
common_spc_track 06_19
Date of last change:2024/09/06
Final Product Information
|
common_outer_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_clean
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Withdrawn(注:已撤市)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