欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FR/H/0499/002
药品名称MONOPROST 50 µg/ml, eye drops solution
活性成分
    • latanoprost 50.0 µg/ml
剂型Eye drop solution in single dose containers
上市许可持有人Laboratoires THEA 12, rue Louis Blériot 63017 Clermont Ferrand Cedex 2 FRANCE
参考成员国 - 产品名称France (FR)
Monoprost 50 microgrammes/ml, collyre en solution
互认成员国 - 产品名称
    • Germany (DE)
      Monoprost 50 Mikrogramm/ml Augentropfen, Lösung
    • Denmark (DK)
      Monoprost
    • Belgium (BE)
      Monoprost 50 microgrammes/ml collyre en solution
    • Netherlands (NL)
    • Luxembourg (LU)
      Monoprost, 50 mcg / 1mL, Collyre en solution
    • Iceland (IS)
      Monoprost 50 míkróg/ml Augndropar, lausn
    • Austria (AT)
      Monopost 50 Mikrogramm/ml Augentropfen, Lösung
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
      MONOPROST
    • Sweden (SE)
    • Norway (NO)
      Monoprost
    • Finland (FI)
      Monoprost 50 mg/ml silmätipat, liuos
    • Poland (PL)
      Monoprost
    • Bulgaria (BG)
      Monoprost
    • Cyprus (CY)
    • Czechia (CZ)
      Monopost 50 mikrogramů/ml
    • Romania (RO)
      MONOPOST 50 micrograme/ml picături oftalmice, soluţie
    • Slovakia (SK)
      MONOPOST 50 mikrogramov/ml očná roztoková instilácia
    • Slovenia (SI)
许可日期2016/10/13
最近更新日期2024/03/13
药物ATC编码
    • S01EE01 latanoprost
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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