欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0365/004
药品名称
Escitalopram Zdrovit
活性成分
escitalopram oxalate 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Former RMS: PT/H/1072 Natur Produkt Zdrovit Sp. z o.o.
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
许可日期
2014/01/21
最近更新日期
2017/07/20
药物ATC编码
N06AB10 escitalopram
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
PubAR
|
575960_575961_575962_575963_20140616_PAR_GBB
Date of last change:2024/09/06
Final Product Information
|
common_impack_10mg
Date of last change:2024/09/06
Final Product Information
|
common_impack_15mg
Date of last change:2024/09/06
Final Product Information
|
common_impack_20mg
Date of last change:2024/09/06
Final Product Information
|
common_impack_5mg
Date of last change:2024/09/06
Final Product Information
|
common_outer_10mg
Date of last change:2024/09/06
Final Product Information
|
common_outer_15mg
Date of last change:2024/09/06
Final Product Information
|
common_outer_20mg
Date of last change:2024/09/06
Final Product Information
|
common_outer_5mg
Date of last change:2024/09/06
Final Product Information
|
common_pl_10mg
Date of last change:2024/09/06
Final Product Information
|
common_pl_15mg
Date of last change:2024/09/06
Final Product Information
|
common_pl_20mg
Date of last change:2024/09/06
Final Product Information
|
common_pl_5mg
Date of last change:2024/09/06
Final Product Information
|
common_spc
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase