欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/7994/002
药品名称
Seretide Diskus
活性成分
fluticasone propionate 250.0 µg
salmeterol 50.0 µg
剂型
Inhalation powder, pre-dispensed
上市许可持有人
GlaxoSmithKline AB Sweden
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
Iceland (IS)
Ireland (IE)
Austria (AT)
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Finland (FI)
Estonia (EE)
Hungary (HU)
Cyprus (CY)
Czechia (CZ)
Romania (RO)
Slovakia (SK)
Malta (MT)
Croatia (HR)
Sweden (SE)
许可日期
2008/04/05
最近更新日期
2024/03/15
药物ATC编码
R03AK06 salmeterol and fluticasone
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 PL
|
SE_H_0169_002_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0169_002_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_0169_002_PAR
Date of last change:2024/09/06
PubAR Summary
|
SE_H_0169_002_PAR Summary
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase