欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/2017/002
药品名称
Olmesartan medoxomilo + Amlodipina Macleods
活性成分
amlodipine 5.0 mg
olmesartan medoxomil 40.0 mg
剂型
Film-coated tablet
上市许可持有人
Macleods Pharma España, SLU
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Olmesartan medoxomil/Amlodipine Macleods 40 mg/5 mg Filmtabletten
Spain (ES)
Italy (IT)
许可日期
2021/07/14
最近更新日期
2023/06/22
药物ATC编码
C09DB02 olmesartan medoxomil and amlodipine
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
Final Product Information
|
common-impack
Date of last change:2021/07/15
Final Product Information
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common-outer
Date of last change:2021/07/15
Final Product Information
|
common-pl
Date of last change:2021/07/15
Final Product Information
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common-spc
Date of last change:2021/07/15
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase