欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3069/001
药品名称Lecartin 50 mg/12,5 mg /200 mg, film-coated tablets
活性成分
    • carbidopa 12.5 mg
    • entacapone 200.0 mg
    • levodopa 50.0 mg
剂型Film-coated tablet
上市许可持有人PharmaSwiss Česká republika s.r.o. Jankovcova 1569/2c, Praha 7 170 00 Czech Republic
参考成员国 - 产品名称Netherlands (NL)
Lecartin 50 mg/ 12,5, mg/ 200 mg filmomhulde tabetten
互认成员国 - 产品名称
    • Lithuania (LT)
    • Estonia (EE)
    • Greece (GR)
      LECARTIN
    • Hungary (HU)
    • Latvia (LV)
    • Slovenia (SI)
    • Slovakia (SK)
许可日期2014/10/01
最近更新日期2014/10/02
药物ATC编码
    • N04BA03 levodopa, decarboxylase inhibitor and COMT inhibitor
申请类型
  • TypeLevel1:Abridged
  • 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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