欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1849/002
药品名称
Amlodipina Valsartan FP
活性成分
amlodipine maleate 5.0 mg
valsartan 160.0 mg
剂型
Film-coated tablet
上市许可持有人
Farmaprojects, S.A.U.
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
2021/10/04
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
PubAR
|
626202_626222_626242_20180702_PAR_ACM
Date of last change:2024/09/06
Final Product Information
|
common_impack_10_160
Date of last change:2024/09/06
Final Product Information
|
common_impack_5_160
Date of last change:2024/09/06
Final Product Information
|
common_impack_5_80_doc
Date of last change:2024/09/06
Final Product Information
|
common_outer_10_160
Date of last change:2024/09/06
Final Product Information
|
common_outer_5_160
Date of last change:2024/09/06
Final Product Information
|
common_outer_5_80
Date of last change:2024/09/06
Final Product Information
|
common_pl_d160
Date of last change:2024/09/06
Final Product Information
|
common_spc_d160
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase