欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号SE/V/0120/001
药品名称Equibactin vet.
活性成分
    • sulfadiazine 250.0 mg/g
    • trimethoprim 50.0 mg/g
剂型Oral powder
上市许可持有人Dechra Regulatory B.V. Netherlands
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Germany (DE)
      Equibactin
    • Belgium (BE)
      Equibactin 250 mg/g + 50 mg/g
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      Equibactin 250 mg/g + 50 mg/g Pulver zum Eingeben für Pferde
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Norway (NO)
      Equibactin vet
    • Poland (PL)
    • Latvia (LV)
      Equibactin vet. 250 mg/g + 50 mg/g pulveris iekšķīgai lietošanai zirgiem
    • Lithuania (LT)
    • Estonia (EE)
      Equibactin vet.
    • Hungary (HU)
    • Cyprus (CY)
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
    • Croatia (HR)
许可日期2019/02/06
最近更新日期2020/06/10
药物ATC编码
    • QJ01EW10 sulfadiazine and trimethoprim
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：Generic - art 13.2 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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