欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/1402/001
药品名称Lecrolyn sine
活性成分
    • sodium cromoglicate 40.0 mg/ml
剂型Eye drops, solution
上市许可持有人Santen Oy, Finland
参考成员国 - 产品名称Sweden (SE)
508870
互认成员国 - 产品名称
    • Belgium (BE)
    • Netherlands (NL)
    • Italy (IT)
    • Poland (PL)
      Lecrolyn
    • Latvia (LV)
      Lecrolyn sine 40 mg/ml acu pilieni, šķīdums
    • Hungary (HU)
      LECROLYN 40 mg/ml oldatos szemcsepp
    • Bulgaria (BG)
    • Czechia (CZ)
      Lecrolyn sine 40 mg/ml oční kapky, roztok
    • Romania (RO)
      Lecrolyn 40 mg/ml picături oftalmice, soluţie
    • Slovakia (SK)
    • Denmark (DK)
    • Iceland (IS)
      Lecrolyn sine 40 mg/ml Augndropar, lausn
    • Norway (NO)
      Lecrolyn sine
    • Finland (FI)
    • Lithuania (LT)
      Lecrolyn sine 40 mg/ml akių lašai (tirpalas)
    • Estonia (EE)
      LECROLYN SINE
许可日期2015/02/24
最近更新日期2023/06/19
药物ATC编码
    • S01GX01 cromoglicic acid
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Non Prescription (including OTC)
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市场状态Positive
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