欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0848/002
药品名称
Escitalopram Zentiva
活性成分
escitalopram oxalate 10.0 mg
剂型
Orodispersible tablet
上市许可持有人
Sanofi-Aventis Prod. Farmacêuticos, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Slovakia (SK)
Italy (IT)
Greece (GR)
Hungary (HU)
ESCITALOPRAM-ZENTIVA 10 mg szájban diszpergálódó tabletta
许可日期
2013/09/06
最近更新日期
2023/12/13
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
PAR
|
56108_56109_56110_56111_20141125_PAR_GBB
Date of last change:2014/12/20
Final Product Information
|
common-spc-day202-clean
Date of last change:2014/12/20
Final Product Information
|
common-impack-day202-clean
Date of last change:2014/12/20
Final Product Information
|
common-outer-day202-clean
Date of last change:2014/12/20
Final Product Information
|
common-pl-day202-clean
Date of last change:2014/12/20
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase