欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0897/001
药品名称
Escitalopram Apotex
活性成分
escitalopram oxalate 5.0 mg
剂型
Orodispersible tablet
上市许可持有人
Apotex Europe, B.V.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Poland (PL)
ApoEscitaxin
许可日期
2013/08/26
最近更新日期
2024/04/24
药物ATC编码
N06AB10 escitalopram
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
|
56041_56042_56043_56044_20141105_PAR_GBB
Date of last change:2024/09/06
Final Product Information
|
common_impack_day 106 clean
Date of last change:2024/09/06
Final Product Information
|
common_outer_day106 clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_day196_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_day196_clean
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase