欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1583/003
药品名称
Candesartan + Hidroclorotiazida Bluefish
活性成分
candesartancilexetil 32.0 mg
hydrochlorothiazide 12.5 mg
剂型
Tablet
上市许可持有人
Bluefish Pharmaceuticals AB
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2016/12/07
最近更新日期
2021/05/07
药物ATC编码
C09DA06 candesartan and diuretics
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
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
|
604042_604043_604044_604045_20161230_PAR_ACM
Date of last change:2024/09/06
Final Product Information
|
Candesartan _ HCTZ Bluefish_Label_clean
Date of last change:2024/09/06
Final Product Information
|
Candesartan _ HCTZ Bluefish_PIL_clean
Date of last change:2024/09/06
Final Product Information
|
Candesartan _ HCTZ Bluefish_SPC_clean
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase