欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号LT/H/0134/001
药品名称Leverette 0,15 mg / 0,03 mg plėvele dengtos tabletės
活性成分
    • ethinyl estradiol 30.0 µg
    • Levonorgestrel 150.0 µg
剂型Film-coated tablet
上市许可持有人UAB Exeltis Baltics Islandijos pl. 209a Kaunas 49163 Lithuania
参考成员国 - 产品名称Lithuania (LT)
互认成员国 - 产品名称
    • Sweden (SE)
    • Denmark (DK)
    • Norway (NO)
    • Iceland (IS)
    • Italy (IT)
    • Austria (AT)
      Leverette 150 Mikrogramm / 30 Mikrogramm Filmtabletten
    • Latvia (LV)
      Leverette 0,15 mg/0,03 mg apvalkotās tabletes
    • Estonia (EE)
      LEVERETTE
    • Hungary (HU)
      MISSEE 0,15 mg/0,03 mg filmtabletta
    • Czechia (CZ)
      Zinnia 0.150 mg / 0.030 mg film-coated tablets
    • Slovakia (SK)
      Leverette 0,15mg/0,03mg filmom obalené tablety
    • Poland (PL)
      Leverette
    • Germany (DE)
    • Belgium (BE)
    • Luxembourg (LU)
许可日期2019/07/02
最近更新日期2025/01/29
药物ATC编码
    • G03AA07 levonorgestrel and ethinylestradiol
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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