欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/4922/002
药品名称
Human Albumin 200 g/l Baxalta
活性成分
albumin human 200.0 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 LBUMIN 200 g/l Baxalta
互认成员国 - 产品名称
Denmark (DK)
Slovakia (SK)
Slovenia (SI)
Malta (MT)
Netherlands (NL)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Italy (IT)
Greece (GR)
Sweden (SE)
Norway (NO)
Poland (PL)
Human Albumin 200 g/l Baxter
Latvia (LV)
Lithuania (LT)
ALBUMIN Baxter 200 g/l infuzinis tirpalas
Estonia (EE)
ALBUMIN BAXALTA 200G/L
Bulgaria (BG)
Cyprus (CY)
Czechia (CZ)
Romania (RO)
ALBUMINA UMANA BAXTER 200 g/l, solutie perfuzabila
Finland (FI)
Portugal (PT)
Hungary (HU)
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
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European Union HMA Authorisation of Medicines DataBase