欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1703/002
药品名称
Febuxostate Oara
活性成分
febuxostat 120.0 mg
剂型
Film-coated tablet
上市许可持有人
Bluepharma - Indústria Farmacêutica, S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Febuxostat Bluepharma 120 mg Filmtabletten
United Kingdom (Northern Ireland) (XI)
许可日期
2017/06/28
最近更新日期
2024/05/14
药物ATC编码
M04AA03 febuxostat
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
PubAR
|
1703_Febuxostate_Oara_PAR_FINAL_11Abril2018
Date of last change:2024/09/06
Final Product Information
|
common_impack_febuxo120
Date of last change:2024/09/06
Final Product Information
|
common_impack_febuxo80
Date of last change:2024/09/06
Final Product Information
|
common_outer_febuxo120_clean
Date of last change:2024/09/06
Final Product Information
|
common_outer_febuxo80_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl
Date of last change:2024/09/06
Final Product Information
|
common_spc_febuxo120_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_febuxo80_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase