欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0872/001
药品名称Eltrombopag Krka 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KRKA, d.d., Novo mesto Šmarješka cesta 6 8501 Novo mesto Slovenia
参考成员国 - 产品名称Hungary (HU)
互认成员国 - 产品名称
    • Denmark (DK)
      Eltrombopag ”Krka”
    • Poland (PL)
      Eltrombopag Krka
    • Belgium (BE)
    • Latvia (LV)
    • Netherlands (NL)
    • Lithuania (LT)
      Eltrombopag Krka 25 mg plėvele dengtos tabletės
    • Iceland (IS)
    • Estonia (EE)
    • Ireland (IE)
    • Czechia (CZ)
      Eltrombopag Krka
    • Austria (AT)
    • Slovakia (SK)
    • France (FR)
    • Slovenia (SI)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Germany (DE)
      Eltrombopag-TAD 25 mg Filmtabletten
    • Finland (FI)
许可日期2024/04/29
最近更新日期2024/11/05
药物ATC编码
    • B02BX05 eltrombopag
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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    市场状态Positive
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