欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/0385/001
药品名称
Olmes 10 mg
活性成分
Olmesartan medoxomil 10.0 mg
剂型
Film-coated tablet
上市许可持有人
Daiichi Sankyo Europe GmbH Zielstattstr. 48 81379 München Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Spain (ES)
Italy (IT)
许可日期
2003/03/30
最近更新日期
2024/12/04
药物ATC编码
C09CA08 olmesartan medoxomil
申请类型
TypeLevel1:
New Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier Article 4.8 Di 65/65
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Product Information
|
final_common_outer_0385_053
Date of last change:2024/09/06
Final Product Information
|
final_common_pl_0385_053
Date of last change:2024/09/06
Final Product Information
|
final_common_spc_0385_053
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase