欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/4708/001
药品名称Bronchipret TP
活性成分
    • thyme herb 100.0 mg
    • PRIMULAE RADIX 60.0 mg
剂型Film-coated tablet
上市许可持有人Bionorica SE Kerschensteinerstr. 11-15 D-92318 Neumark Germany
参考成员国 - 产品名称Germany (DE)
Bronchipret TP
互认成员国 - 产品名称
    • Italy (IT)
    • Hungary (HU)
      BRONCHIPRET filmtabletta
    • Denmark (DK)
      Mucopret
    • Netherlands (NL)
    • Luxembourg (LU)
    • Austria (AT)
      Bronchithym Filmtabletten
    • France (FR)
    • Spain (ES)
    • Sweden (SE)
    • Poland (PL)
      Bronchitabs
    • Latvia (LV)
      Mucopret apvalkotās tabletes
    • Lithuania (LT)
      Bronchipret plėvele dengtos tabletės
    • Estonia (EE)
      BRONCHIPRET THYME & PRIMULA
    • Bulgaria (BG)
      Bronchipret TP
    • Romania (RO)
    • Slovakia (SK)
      Mucopret
    • Slovenia (SI)
    • Croatia (HR)
      Bronchipret TP filmom obložene tablete
许可日期2017/10/04
最近更新日期2023/08/18
药物ATC编码
    • R05CA10 combinations
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4：Herbal
  • TypeLevel5：Non Prescription (including OTC)
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市场状态Positive
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