欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4002/003
药品名称Dasatinib Sandoz 70 mg, filmomhulde tabletten
活性成分
    • Dasatinib 70.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Hospitaaldreef 29 1315 RC Almere Nederland
参考成员国 - 产品名称Netherlands (NL)
Dasatinib Sandoz 70 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Czechia (CZ)
      Dasatinib Sandoz
    • Denmark (DK)
      Dasatinib "Sandoz"
    • Estonia (EE)
    • Norway (NO)
    • Germany (DE)
      Dasatinib PharOS 70 mg Filmtabletten
    • Belgium (BE)
      Dasatinib Sandoz 70 mg filmomhulde tabletten
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Italy (IT)
    • Sweden (SE)
    • Finland (FI)
    • Latvia (LV)
      Dasatinib Sandoz 70 mg apvalkotās tabletes
    • Lithuania (LT)
      Dasatinib Sandoz 70 mgplėvele dengtos tabletės
    • Hungary (HU)
      DASATINIB SANDOZ 70 mg filmtabletta
    • Romania (RO)
      Dasatinib Sandoz 70 mg comprimate filmate
    • Slovakia (SK)
      Dasatinib PharOS 70 mg
    • Slovenia (SI)
      Dasatinib Sandoz 70 mg filmsko obložene tablete
许可日期2018/07/25
最近更新日期2025/01/28
药物ATC编码
    • L01XE06 dasatinib
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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