欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/1580/001
药品名称Dolenio
活性成分
    • glucosamine 1178.0 mg
剂型Film-coated tablet
上市许可持有人Blue Bio Pharmaceuticals Limited 5th Floor, Beaux Lane House, Mercer Street Lower Dublin2 Republic of Ireland
参考成员国 - 产品名称Denmark (DK)
Dolenio
互认成员国 - 产品名称
    • Germany (DE)
      Dolenio Filmtabletten
    • Belgium (BE)
    • Netherlands (NL)
      Dolenio
    • Luxembourg (LU)
    • Iceland (IS)
    • Ireland (IE)
    • Austria (AT)
      Bolevo 1500 mg Filmtabletten
    • France (FR)
    • Portugal (PT)
    • Greece (GR)
    • Poland (PL)
    • Estonia (EE)
      BONARTOS
    • Hungary (HU)
      DOLENIO 1500 mg filmtabletta
    • Bulgaria (BG)
      Bonartos
    • Cyprus (CY)
      DOLENIO FC TABS
    • Czechia (CZ)
      BAYFLEX 1178 MG
    • Romania (RO)
      Slideflex 1178 mg comprimate filmate
    • Malta (MT)
许可日期2008/12/23
最近更新日期2023/04/18
药物ATC编码
    • M01AX05 glucosamine
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Bibliographic Art 10 a Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Non Prescription (including OTC)
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市场状态Positive
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