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)
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2024/01/22
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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