欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
AT/H/0683/001
药品名称
Flexbumin
活性成分
albumin human 200.0 g/l
剂型
Solution for infusion
上市许可持有人
Baxalta Innovations GmbH, Austria
参考成员国 - 产品名称
Austria (AT)
Flexbumin 200 g/l - Infusionslösung
互认成员国 - 产品名称
Denmark (DK)
Flexbumin
Malta (MT)
Flexbumin 200g/l
Netherlands (NL)
Flexbumin 200 g/l, oplossing voor infusie
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Norway (NO)
Poland (PL)
Flexbumin 200 g/l
Latvia (LV)
Flexbumin 200 g/l šķīdums infūzijām
Lithuania (LT)
Flexbumin 200 g/l infuzinis tirpalas
Estonia (EE)
FLEXBUMIN 200 G/L
Hungary (HU)
Flexbumin 200 g/l oldatos infúzió
Cyprus (CY)
flexbumin 200g/l 27M0014
Czechia (CZ)
Flexbumin 200 g/l
Slovakia (SK)
Flexbumin 200 g/l
Slovenia (SI)
许可日期
2008/04/05
最近更新日期
2024/12/23
药物ATC编码
B05AA01 albumin
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
|
AT_H_0683_PAR_Flexbumin solution for infusion
Date of last change:2025/01/02
Final SPC
|
Common English SmPC_ Flexbumin_ 250 gl_ solution for infusion_ EU_ _en__ Feb_2023_2
Date of last change:2024/09/06
Final Labelling
|
common_lab_flexbumin_200gl_IS comments_clean
Date of last change:2024/09/06
Final Labelling
|
common_lab_flexbumin_250gl_IS comments_clean
Date of last change:2024/09/06
Final PL
|
common_pl_flexbumin200glsolutionforinfusionclean
Date of last change:2024/09/06
Final PL
|
common_pl_flexbumin250glsolutionforinfusionclean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase