欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/4922/001
药品名称
Human Albumin 50 g/l Baxalta
活性成分
albumin human 50.0 g/l
剂型
Solution for infusion
上市许可持有人
Takeda GmbH
参考成员国 - 产品名称
Germany (DE)
HUMAN ALBUMIN 50 g/l Baxalta
互认成员国 - 产品名称
Poland (PL)
Denmark (DK)
Malta (MT)
Belgium (BE)
Luxembourg (LU)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Italy (IT)
Greece (GR)
Sweden (SE)
Norway (NO)
Latvia (LV)
Lithuania (LT)
ALBUMIN Baxter 50 g/l infuzinis tirpalas
Estonia (EE)
ALBUMIN BAXALTA 50G/L
Bulgaria (BG)
Cyprus (CY)
Romania (RO)
ALBUMINA UMANA BAXTER 50 g/l, solutie perfuzabila
Slovenia (SI)
Finland (FI)
许可日期
2008/04/05
最近更新日期
2025/01/14
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
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase