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
2024/12/20
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
PubAR
|
Final PAR Flynise 5 mg filmcoated tablets DKH2384_001_DC
Date of last change:2024/09/06
PubAR Summary
|
Final sPAR Flynise 5 mg filmcoated tablets DKH2384_001_DC
Date of last change:2024/09/06
Final PL
|
PI_Desloratadine FCT_DK_H_2384_01_V003G_v2_1_020317_CL
Date of last change:2024/09/06
Final Product Information
|
PI_Desloratadine_FCT_DK_H_2384_01_V006_v4_1_151117_CL
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase