欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1596/001
药品名称
Solifenacina Demo
活性成分
solifenacin succinate 5.0 mg
剂型
Film-coated tablet
上市许可持有人
Demo, SA
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Greece (GR)
SOLIFENACIN/DEMO
许可日期
2017/02/15
最近更新日期
2023/09/04
药物ATC编码
G04BD08 solifenacin
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
|
1596_PAR_Final_05DEZ2018
Date of last change:2024/09/06
Final Product Information
|
common_labelling_10mg
Date of last change:2024/09/06
Final Product Information
|
common_labelling_5mg
Date of last change:2024/09/06
Final Product Information
|
common_pil
Date of last change:2024/09/06
Final Product Information
|
common_spc_10mg
Date of last change:2024/09/06
Final Product Information
|
common_spc_5mg
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase