欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/0808/001
药品名称Nefopam Hydrochloride 30 mg Film-coated Tablets
活性成分
    • nefopam hydrochloride 30.0 mg
剂型Film-coated tablet
上市许可持有人Key Pharmaceuticals Ltd Galen House 83 High Street Somersham Cambridgeshire PE28 3JB UK
参考成员国 - 产品名称Ireland (IE)
Nefopam Hydrochloride
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
许可日期2020/12/02
最近更新日期2020/12/02
药物ATC编码
    • N02BG06 nefopam
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
附件文件下载
    市场状态Positive
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