欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/2087/001
药品名称
Telmisartan + Hidroclorotiazida Aristo
活性成分
hydrochlorothiazide 12.5 mg
telmisartan 40.0 mg
剂型
Tablet
上市许可持有人
Aristo Pharma Iberia, SL
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2018/11/05
最近更新日期
2024/02/28
药物ATC编码
C09DA07 telmisartan 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
PubAR
|
2087_Telmisartan_Hidroclorotiazida_Aristo_PAR_09NOV2018_ACM_IRS_ARISTO
Date of last change:2024/09/06
Final Product Information
|
common_impack
Date of last change:2024/09/06
Final Product Information
|
common_outpack
Date of last change:2024/09/06
Final Product Information
|
common_pl_ 80_25mg_D106
Date of last change:2024/09/06
Final Product Information
|
common_pl_40_80_12_5 mg_D106
Date of last change:2024/09/06
Final Product Information
|
common_spc_ 80_25 mg_D106
Date of last change:2024/09/06
Final Product Information
|
common_spc_40 _ 80_12_5 mg_D106
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase