欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1861/004
药品名称
Olmesartan medoxomilo + Hidroclorotiazida Jubilant
活性成分
hydrochlorothiazide 25.0 mg
olmesartan medoxomil 40.0 mg
剂型
Film-coated tablet
上市许可持有人
Jubilant Pharmaceuticals NV
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Spain (ES)
许可日期
2018/08/22
最近更新日期
2021/07/08
药物ATC编码
C09DA08 olmesartan medoxomil 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
|
1861_Olmesartan_medoxomilo_Hidroclorotiazida_Jubilant_PAR_ACM_final
Date of last change:2024/09/06
Final Product Information
|
common_labelling_impack
Date of last change:2024/09/06
Final Product Information
|
common_labelling_outer
Date of last change:2024/09/06
Final Product Information
|
common_pl 20_12_5mg _ 20_25mg
Date of last change:2024/09/06
Final Product Information
|
common_pl 40_12_5mg _ 40_25mg
Date of last change:2024/09/06
Final Product Information
|
common_smpc 20_12_5mg _ 20_25mg
Date of last change:2024/09/06
Final Product Information
|
common_smpc 40_12_5mg _ 40_25mg
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase