欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0852/002
药品名称Pazopanib Viatris 400 mg Film-coated tablet
活性成分
    • PAZOPANIB hydrochloride 400.0 mg
剂型Film-coated tablet
上市许可持有人VIATRIS Limited Damastown Road Damastown Industrial Park Dublin 15 County Co. Dublin D15 XD71 Ireland E-mail mylanireland.mahs
参考成员国 - 产品名称Hungary (HU)
互认成员国 - 产品名称
    • Iceland (IS)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Norway (NO)
    • Poland (PL)
      Pazopanib Viatris
    • Latvia (LV)
    • Germany (DE)
      Pazopanib Viatris 400 mg Filmtabletten
    • Lithuania (LT)
      Pazopanib Viatris 400 mg plėvele dengtos tabletės
    • Denmark (DK)
    • Estonia (EE)
    • Belgium (BE)
    • Czechia (CZ)
      Pazopanib Viatris
    • Netherlands (NL)
    • Luxembourg (LU)
许可日期2024/01/24
最近更新日期2024/01/29
药物ATC编码
    • L01EX03 pazopanib
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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