欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号FI/H/0914/001
药品名称Hydrocortisone Panpharma
活性成分
    • HYDROCORTISONE SODIUM SUCCINATE succinate 133.7 mg
剂型Powder and solvent for solution for injection
上市许可持有人Panpharma Z.I. du Clairay 35133 LUITRÉ France
参考成员国 - 产品名称Finland (FI)
Hydrocortisone Panpharma
互认成员国 - 产品名称
    • Sweden (SE)
    • Poland (PL)
    • Romania (RO)
      Hidrocortizon Panpharma 100 mg pulbere și solvent pentru soluție injectabilă/perfuzabilă
许可日期2018/02/05
最近更新日期2024/07/11
药物ATC编码
    • H02AB09 hydrocortisone
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial 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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