欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/V/0121/001
药品名称Phenoxypen WSP
活性成分
    • phenoxymethylpenicillin potassium salt 325.0 mg/g
剂型Powder for oral solution
上市许可持有人Dopharma Research BV Zalmweg Raamsdonskveer The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Phenoxypen WSP
互认成员国 - 产品名称
    • Germany (DE)
    • Denmark (DK)
      Phenoxylin
    • Belgium (BE)
      Phenoxypen WSP
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
      PHENOXYPEN WSP
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Poland (PL)
    • Lithuania (LT)
      PHENOXYPEN 325 mg/g, milteliai geriamajam tirpalui ruošti viščiukams
    • Hungary (HU)
    • Czechia (CZ)
    • Slovakia (SK)
    • Bulgaria (BG)
      Phenoxypen WSP
    • Romania (RO)
许可日期2006/10/25
最近更新日期2021/10/07
药物ATC编码
    • QJ01CE02 phenoxymethylpenicillin
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：Full dossier Art 12.3 (j) Dir 2001/82/EC
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
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