欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号PT/H/0618/001
药品名称Paracetamol Basi
活性成分
    • paracetamol 40.0 mg/ml
剂型Syrup
上市许可持有人Laboratórios Basi - Industria Farmacêutica, SA Coimbra Portugal
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Czechia (CZ)
    • Belgium (BE)
      Paracetamol Teva 40 mg/ml suspensie voor oraal gebruik
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Paracetamol Basi 40 mg/ml Sirup
    • Latvia (LV)
      APAPKIT 40 mg/ml suspensija iekšķīgai
    • Estonia (EE)
      PARACETAMOL BASI 40 MG/ML
    • Hungary (HU)
      SUPOFEN 40 mg/ml belsőleges szuszpenzió
    • Bulgaria (BG)
      Paracetamol Basi
    • Romania (RO)
      Supofen 40 mg/ml suspensie orala
    • Slovenia (SI)
      Supofen 40 mg/ml peroralna suspenzija
    • Malta (MT)
      Supofen 200mg/5ml oral suspension
许可日期2012/11/14
最近更新日期2024/04/08
药物ATC编码
    • N02BE01 paracetamol
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
附件文件下载
市场状态Positive
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