欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/H/0313/001
药品名称
RAMIPRIL E IDROCLOROTIAZIDE SUN
活性成分
hydrochlorothiazide 12.5 mg
ramipril 2.5 mg
剂型
Tablet
上市许可持有人
SUN PHARMACEUTICAL INDUSTRIES (EUROPE) B.V.
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
Germany (DE)
Spain (ES)
许可日期
2014/01/14
最近更新日期
2022/01/21
药物ATC编码
C09BA05 ramipril and diuretics
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_pl_v13_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_v13_clean
Date of last change:2024/09/06
Final PL
|
final common_pl_v12_track
Date of last change:2024/09/06
Final SPC
|
final common_spc_v12_track
Date of last change:2024/09/06
Final Product Information
|
notification of approval
Date of last change:2024/09/06
PubAR
|
PAR IT_H_0313_001_002_DC
Date of last change:2024/09/06
市场状态
Positive
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