欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/2004/001
药品名称
Paruda
活性成分
rupatadine 10.0 mg
剂型
Tablet
上市许可持有人
Substipharm Développement
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2018/03/14
最近更新日期
2022/02/04
药物ATC编码
R06AX28 rupatadine
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
|
613422_20180320_PAR_GBB
Date of last change:2024/09/06
PubAR
|
613423_20180320_PAR_GBB
Date of last change:2024/09/06
PubAR
|
621902_20180320_PAR_GBB
Date of last change:2024/09/06
PubAR
|
621903_20180320_PAR_GBB
Date of last change:2024/09/06
PubAR
|
621904_20180320_PAR_GBB
Date of last change:2024/09/06
PubAR
|
621905_20180320_PAR_GBB
Date of last change:2024/09/06
Final Product Information
|
common_impack_d0
Date of last change:2024/09/06
Final Product Information
|
common_outer_d160_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_d160_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_d200_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase