欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/1226/001
药品名称Fludrocortisone Acetate Renata 0.1 mg Tablets
活性成分
    • fludrocortisone acetate 0.1 mg
剂型Tablet
上市许可持有人Renata Pharmaceuticals (Ireland) Limited, (22865), (LOC-100028164), 13-18 City Quay, Dublin 2, Ireland
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Malta (MT)
许可日期2023/10/04
最近更新日期2024/03/22
药物ATC编码
    • H02AA02 fludrocortisone
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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