欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/1777/004
药品名称
Candesartan 32 mg
活性成分
candesartancilexetil 32.0 mg
剂型
Tablet
上市许可持有人
Pharmachemie B.V., Swensweg 5, 2031 GA Haarlem, The Netherlands
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
许可日期
2010/06/25
最近更新日期
2015/02/24
药物ATC编码
C09CA06 candesartan
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
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 Product Information
|
common outer NLH1777
Date of last change:2024/09/06
Final Product Information
|
common PIL NLH1777
Date of last change:2024/09/06
Final Product Information
|
common SmPC NLH1777
Date of last change:2024/09/06
Final PL
|
common_pl_candesartanclean _ final
Date of last change:2024/09/06
Final SPC
|
common_spc_candesartanclean _ final
Date of last change:2024/09/06
Final Labelling
|
Final Label _candesartan_ clean
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
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European Union HMA Authorisation of Medicines DataBase