欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1027/002
药品名称
Escitalopram Bluefish
活性成分
escitalopram oxalate 10.0 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
Spain (ES)
Denmark (DK)
Escitalopram Bluefish
Iceland (IS)
Escitalopram Bluefish 10 mg Filmuhúðuð tafla
Ireland (IE)
Austria (AT)
Escitalopram Bluefish 10 mg Filmtabletten
Sweden (SE)
Poland (PL)
Escitalopram Bluefish
许可日期
2014/01/20
最近更新日期
2022/11/28
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
|
56887_56888_56889_56890_20140822_PAR_GBB
Date of last change:2016/04/26
市场状态
Positive
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