欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/1842/002
药品名称Propofol Pfizer 20 mg/ml
活性成分
    • propofol 20.0 mg/ml
剂型Emulsion for injection or infusion
上市许可持有人Pfizer The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Propofol Pfizer 20 mg/ml
互认成员国 - 产品名称
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Hungary (HU)
    • Belgium (BE)
    • Luxembourg (LU)
    • Italy (IT)
    • Greece (GR)
    • Cyprus (CY)
      PROPOFOL PFIZER 20mg/ml EMULSION FOR INJECTION OR INFUSION
    • Romania (RO)
      Curtega 20 mg/ml emulsie injectabila/perfuzabila
    • Malta (MT)
许可日期2011/05/19
最近更新日期2013/11/15
药物ATC编码
    • N01AX10 propofol
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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    市场状态Positive
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