欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3520/001
药品名称Clopidogrel(sulfaat) CF 75 mg, filmomhulde tabletten
活性成分
    • CLOPIDOGREL SULFATE 75.0 mg
剂型Film-coated tablet
上市许可持有人Centrafarm B.V. Nieuwe Donk 3 4879 AC Etten-Leur The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Clopidogrel(sulfaat) CF 75 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Clopidogrel(sulfat) AL 75 mg Filmtabletten
    • Denmark (DK)
      Clopidogrel (sulfat) Stada
    • Belgium (BE)
      Clopidogrel Eurogenerics 75mg filmomhulde tabletten
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Sweden (SE)
    • Finland (FI)
    • Czechia (CZ)
      CLOPIDOGREL STADA 75 MG POTAHOVANÉ TABLETY
许可日期2016/08/02
最近更新日期2024/02/29
药物ATC编码
    • B01AC04 clopidogrel
申请类型
  • TypeLevel1:Known Active Substance
  • 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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市场状态Positive
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