欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0506/001
药品名称
Asixa
活性成分
triflusal 300.0 mg
剂型
Capsule, hard
上市许可持有人
Glenmark Pharmaceuticals s.r.o
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2011/12/22
最近更新日期
2021/04/30
药物ATC编码
B01AC18 triflusal
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
|
0506_Asixa_Summary_PAR_Scientific_PAR_Final_24ABR2017
Date of last change:2024/09/06
Final Product Information
|
common_labelling_coplat_clean_day195
Date of last change:2024/09/06
Final Product Information
|
common_leaflet_coplat_clean_day209
Date of last change:2024/09/06
Final PL
|
common_leaflet_v002_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_coplat_clean_day209
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase