欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/1510/003
药品名称
Mylopram
活性成分
escitalopram oxalate 15.0 mg
剂型
Film-coated tablet
上市许可持有人
Mylan NM AB Box 23033 SE-104 35 Stockholm Sweden
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
许可日期
2009/07/02
最近更新日期
2017/05/02
药物ATC编码
N06AB10 escitalopram
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final SPC
|
Mylopram _ clean
Date of last change:2024/09/06
PubAR
|
parmod5_dk1510mylopram_pdf
Date of last change:2024/09/06
PubAR
|
pllab_dk1510mylopram_pdf
Date of last change:2024/09/06
Final Labelling
|
Product information
Date of last change:2024/09/06
Final PL
|
Product information_2
Date of last change:2024/09/06
PubAR
|
spc_dk1510mylopram_pdf
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase