欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1337/004
药品名称
Ramipril/Amlodipine Glenmark 10 mg/10 mg
活性成分
Amlodipine besilate 10.0 mg
Ramipril 10.0 mg
剂型
Capsule, hard
上市许可持有人
Glenmark Arzneimittel GmbH Germany
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
许可日期
2014/05/14
最近更新日期
2024/10/29
药物ATC编码
C09BB07 ramipril and amlodipine
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Fixed combination Art 10b Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE_H_1337_004_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1337_004_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1337_004_PAR
Date of last change:2024/09/06
PubAR Summary
|
SE_H_1337_004_PAR Summary
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
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European Union HMA Authorisation of Medicines DataBase