欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/1600/001
药品名称
Ramipril Hexal comp 5 mg/12,5 mg Tabletten
活性成分
Hydrochlorothiazide 12.5 mg
Ramipril 5.0 mg
剂型
Tablet
上市许可持有人
HEXAL AG Industriestr. 25 83607 Holzkirchen Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
许可日期
2009/12/23
最近更新日期
2024/11/20
药物ATC编码
C09BA05 ramipril and diuretics
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Multiple (Copy) Application
TypeLevel3:
Other Generic application Art 10.3 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
PubAR
|
04_DE1597_1603_DC_Ramipril_final PAR
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl_clean_ 937
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl_tracked_ 936
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl_tracked_ 937
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc_clean _ 836
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc_tracked _ 836
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc_tracked _ 838
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase