欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0421/002
药品名称
Xartan HD
活性成分
hydrochlorothiazide 25.0 mg
losartan potassium salt 100.0 mg
剂型
Film-coated tablet
上市许可持有人
Adamed Sp. z.o.o. Pienkow 149 05-152 Czosnow Poland
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
许可日期
2010/02/24
最近更新日期
2019/10/18
药物ATC编码
C09DA01 losartan and diuretics
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final Product Information
|
Final Xartan common clean
Date of last change:2024/09/06
Final Labelling
|
Final Xartan HCT LAB_clean
Date of last change:2024/09/06
Final PL
|
Final Xartan HCT PIL clean
Date of last change:2024/09/06
Final SPC
|
Final Xartan HCT SPC clean
Date of last change:2024/09/06
PubAR
|
parmod5_dk1768zalarloscomp_pdf
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
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European Union HMA Authorisation of Medicines DataBase