欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0899/002
药品名称
Escitalopram Symphar 10 mg
活性成分
escitalopram oxalate 10.0 mg
剂型
Film-coated tablet
上市许可持有人
Symphar Sp. z o.o. Ul. Koszykowa 65 00-667 Warsaw, Poland
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
许可日期
2022/11/15
最近更新日期
2024/02/01
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
Final Labelling
|
common_labelling_clean
Date of last change:2024/09/06
Final PL
|
common_pl_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_clean
Date of last change:2024/09/06
PubAR
|
PAR_SK_H_0284_001_003_DC_Escitalopram Symphar
Date of last change:2024/09/06
PubAR Summary
|
Summary PAR_SK_H_0284_001_003_DC_Escitalopram Symphar
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase