欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1027/004
药品名称
Escitalopram Bluefish
活性成分
Escitalopram oxalate 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Bluefish Pharmaceuticals AB
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Iceland (IS)
Escitalopram Bluefish 20 mg Filmuhúðuð tafla
Ireland (IE)
Poland (PL)
Escitalopram Bluefish
许可日期
2014/01/20
最近更新日期
2025/01/02
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
|
56887_56888_56889_56890_20140822_PAR_GBB
Date of last change:2024/09/06
市场状态
Positive
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