欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0588/002
药品名称
Amlopharm
活性成分
amlodipine mesilate 10.0 mg
剂型
Tablet
上市许可持有人
Stada Arzneimittel AG Stadastrasse 2-18 61118 Bad Vilbel Germany
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
许可日期
2004/02/16
最近更新日期
2019/01/11
药物ATC编码
C08CA01 amlodipine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Other Article 4.8(a)(iii), second paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Labelling
|
1.3.1-Lab-combined-common-en-DK-0588-001-002-cl
Date of last change:2018/03/23
Final PL
|
1.3.1-PL_0588_20180103_cl
Date of last change:2018/03/23
Final SPC
|
1.3.1-SmPC_0588_20180103_cl
Date of last change:2018/03/23
Final Product Information
|
PL_Amlodipine_mesilate_DK588_20160411cl
Date of last change:2016/07/14
Final Product Information
|
SmPC_Amlodipine_mesilate_DK588_20160411cl
Date of last change:2016/07/14
市场状态
Withdrawn(注:已撤市)
©2006-2024
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase