欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5319/002
药品名称Acecort 5 mg, filmcoated tablets
活性成分
    • hydrocortisone 5.0 mg
剂型Film-coated tablet
上市许可持有人ACE Pharmaceuticals BV Schepenveld 41, 3891 ZK Zeewolde The Netherland
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Germany (DE)
      Acecort 5 mg Filmtabletten
    • Denmark (DK)
      Lilinorm
    • Belgium (BE)
      Acecort 5 mg filmomhulde tabletten
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
许可日期2021/09/09
最近更新日期2023/03/10
药物ATC编码
    • H02AB09 hydrocortisone
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Bibliographic Art 10 a Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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