欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0820/001
药品名称Pazopanib Accord 200mg Film-coated tablet
活性成分
    • PAZOPANIB 200.0 mg
剂型Film-coated tablet
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 Utrecht 3526 KV, Netherlands
参考成员国 - 产品名称Hungary (HU)
互认成员国 - 产品名称
    • Finland (FI)
    • Denmark (DK)
    • Poland (PL)
      Pazopanib Accord
    • Belgium (BE)
      Pazopanib Accord 200 mg Filmtabletten
    • Latvia (LV)
    • Netherlands (NL)
      Pazopanib Accord 200 mg filmomhulde tabletten
    • Lithuania (LT)
      Pazopanib Accord 200 mg plėvele dengtos tabletės
    • Ireland (IE)
    • Estonia (EE)
    • France (FR)
    • Bulgaria (BG)
      Pazopanib Accord
    • Spain (ES)
    • Czechia (CZ)
      Pazopanib Accord 200 mg potahované tablety
    • Portugal (PT)
    • Romania (RO)
    • Italy (IT)
    • Slovakia (SK)
    • Greece (GR)
    • Slovenia (SI)
    • Sweden (SE)
    • Croatia (HR)
    • Norway (NO)
许可日期2023/10/24
最近更新日期2023/10/25
药物ATC编码
    • L01EX03 pazopanib
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Multiple (Copy) 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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