欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1848/001
药品名称
Amlodipina + Valsartan Pensa
活性成分
amlodipine maleate 5.0 mg
valsartan 80.0 mg
剂型
Film-coated tablet
上市许可持有人
Tolife, Produtos Farmacêuticos, S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2017/12/06
最近更新日期
2023/03/14
药物ATC编码
C09DB01 valsartan and amlodipine
申请类型
TypeLevel1:
Known Active Substance
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
PAR Summary
|
1848_Summary_PARScientific_PAR_Amlodipina_Valsartan_Pensa_final
Date of last change:2017/12/22
Final Product Information
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common-spc-d160
Date of last change:2017/12/22
Final Product Information
|
common-impack-5-80.doc
Date of last change:2017/12/22
Final Product Information
|
common-outer-5-80
Date of last change:2017/12/22
Final Product Information
|
common-impack-5-160
Date of last change:2017/12/22
Final Product Information
|
common-impack-10-160
Date of last change:2017/12/22
Final Product Information
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common-outer-5-160
Date of last change:2017/12/22
Final Product Information
|
common-outer-10-160
Date of last change:2017/12/22
Final Product Information
|
common-pl-d160
Date of last change:2017/12/22
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase