欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0412/003
药品名称
Escitomar 20mg tablets
活性成分
escitalopram oxalate 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Genthon BV Microweg 22 6545 CM Nijmegen The Netherlands
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
Ireland (IE)
Escitomar 20 mg film-coated tablets
许可日期
2010/08/11
最近更新日期
2016/07/07
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 SPC
|
M13_1_01_ECM_hox_tab_002_08_Core
Date of last change:2024/09/06
Final Labelling
|
M13_1_02_ECM_hox_tab_002_06_lAB
Date of last change:2024/09/06
Final PL
|
M13_1_03_ECM_hox_tab_002_09_PIL
Date of last change:2024/09/06
PubAR
|
PAR _ Escitomar
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase