欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1180/001
药品名称
Olmesartan Aurobindo
活性成分
Olmesartan medoxomil 10.0 mg
剂型
Film-coated tablet
上市许可持有人
Aurobindo Pharma (Portugal), Unipessoal Limitada
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Malta (MT)
Olmesartan 10mg film-coated tablets
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
许可日期
2014/07/24
最近更新日期
2024/12/24
药物ATC编码
C09CA08 olmesartan medoxomil
申请类型
TypeLevel1:
Abridged
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
Final Labelling
|
Clean_Labelling_11_07_2014
Date of last change:2024/09/06
Final PL
|
Clean_PIL_11_07_2014
Date of last change:2024/09/06
Final SPC
|
Clean_SPC_05_02_2014
Date of last change:2024/09/06
PubAR
|
Olmesartan_Aurobindo_PAR_Scientific_discussion_DEZ2014_IRS
Date of last change:2024/09/06
PubAR
|
Olmesartan_Aurobindo_Summary_PAR_DEZ2014_IRS
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase