欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FI/H/0665/001
药品名称Anya
活性成分
    • Ethinylestradiol 20.0 µg
    • Levonorgestrel 90.0 µg
剂型Film-coated tablet
上市许可持有人Wyeth AB P.O. Box 1822 17124 Solna Sweden
参考成员国 - 产品名称Finland (FI)
互认成员国 - 产品名称
    • Germany (DE)
      Anya Filmtablette
    • Denmark (DK)
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Cyprus (CY)
      ANYA
许可日期2008/09/18
最近更新日期2024/12/12
药物ATC编码
    • G03AA07 levonorgestrel and ethinylestradiol
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
    市场状态Positive
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