欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1487/002
药品名称
Ramipril Ritisca
活性成分
Ramipril 2.5 mg
剂型
Tablet
上市许可持有人
Aurovitas Unipessoal, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Belgium (BE)
Ramipril AB 2,5 mg tabletten
Netherlands (NL)
Poland (PL)
Ramipril Aurovitas
许可日期
2016/09/21
最近更新日期
2024/11/20
药物ATC编码
C09AA05 ramipril
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
|
599844_599847_599845_599846_20161018_PAR_ACM
Date of last change:2024/09/06
Final Product Information
|
Labelling
Date of last change:2024/09/06
Final Product Information
|
PIL
Date of last change:2024/09/06
Final Product Information
|
SPC
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase