欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1147/002
药品名称
Amlodipina Dr. Max
活性成分
amlodipine besilate 10.0 mg
剂型
Tablet
上市许可持有人
Dr. Max Pharma Limited
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2014/09/24
最近更新日期
2019/02/01
药物ATC编码
C08CA01 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
|
Amlodipina_Dr_Max_Summary_PAR_Scientific_PAR07JAN2016_rev160119
Date of last change:2024/09/06
Final Product Information
|
common_impack_5_10 mg_140305_clean
Date of last change:2024/09/06
Final Product Information
|
common_outer_5_10mg_140305_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_5_10mg_140305_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_amlodipine5_10mg_140731_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase