欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5698/002
药品名称Eltrombopag Genthon 25 mg, film-coated tablets
活性成分
    • Eltrombopag 25.0 mg
剂型Film-coated tablet
上市许可持有人Genthon B.V. Microweg 22 6545 CM Nijmegen The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Eltrombopag Genthon 25 mg, tabletten
互认成员国 - 产品名称
    • Poland (PL)
      Eltrombopag Sandoz
    • Croatia (HR)
    • Denmark (DK)
      Eltrombopag Sandoz
    • Latvia (LV)
    • Ireland (IE)
    • Lithuania (LT)
      Eltrombopag Sandoz 25 mg plėvele dengtos tabletės
    • Austria (AT)
    • Estonia (EE)
    • France (FR)
    • Hungary (HU)
    • Spain (ES)
    • Bulgaria (BG)
    • Italy (IT)
    • Cyprus (CY)
      Eltrombopag/Sandoz 25 mg film-coated tablets
    • Greece (GR)
    • Czechia (CZ)
      Eltrombopag Sandoz
    • Sweden (SE)
    • Romania (RO)
    • Norway (NO)
    • Slovakia (SK)
    • Malta (MT)
      Eltrombopag Genthon 25 mg film-coated tablets
    • Finland (FI)
    • Slovenia (SI)
    • Germany (DE)
      Eltrombopag - 1 A Pharma 25 mg Filmtabletten
许可日期2024/01/08
最近更新日期2025/01/28
药物ATC编码
    • B02BX05 eltrombopag
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
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