欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2280/001
药品名称Femoston-conti
活性成分
    • 1. Estradiol hemihydrate 1.0 mg
    • Dydrogesterone 5.0 mg
剂型Film-coated tablet
上市许可持有人Abbott B.V. Wegalaan 9 2132 JD Hoofddorp Nederland
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Germany (DE)
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Denmark (DK)
    • Austria (AT)
      Femoston conti 1 mg/5 mg Filmtabletten
    • Norway (NO)
    • Portugal (PT)
    • Slovenia (SI)
    • Italy (IT)
    • Spain (ES)
    • Finland (FI)
    • Sweden (SE)
许可日期2008/04/05
最近更新日期2024/11/12
药物ATC编码
    • G03FA Progestogens and estrogens, fixed combinations
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
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