欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FI/H/1077/001
药品名称
Flynise
活性成分
desloratadine 5.0 mg
剂型
Film-coated tablet
上市许可持有人
Actavis Group PTC ehf. Reykjavíkurvegur 76-78 220 Hafnarfjordur Iceland
参考成员国 - 产品名称
Finland (FI)
互认成员国 - 产品名称
Iceland (IS)
Flynise 5 mg Filmuhúðuð tafla
Sweden (SE)
Norway (NO)
Flynise
Poland (PL)
AlergoTeva
许可日期
2015/01/16
最近更新日期
2023/05/24
药物ATC编码
R06AX27 desloratadine
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final Product Information
|
PI-Desloratadine_FCT-DK_H_2384_01-V006-v4.1-151117-CL
Date of last change:2018/03/16
Final PL
|
PI-Desloratadine FCT-DK_H_2384_01-V003G-v2.1-020317-CL
Date of last change:2017/06/09
PAR Summary
|
Final sPAR Flynise 5 mg filmcoated tablets DKH2384_001_DC
Date of last change:2016/01/26
PAR
|
Final PAR Flynise 5 mg filmcoated tablets DKH2384_001_DC
Date of last change:2016/01/26
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase