欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FR/V/0196/001
药品名称BYEMITE 500 mg/ml Concentrate for spraying emulsion for laying hens
活性成分
    • phoxim 500.0 mg/mL
剂型Cutaneous solution
上市许可持有人Bayer Animal Health
参考成员国 - 产品名称France (FR)
BYEMITE
互认成员国 - 产品名称
    • Belgium (BE)
      BE-V333837
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
      Baymite Vet. 500 mg/ml handa varphænum
    • Ireland (IE)
    • Austria (AT)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
      Baymite vet
    • Finland (FI)
    • Hungary (HU)
    • Bulgaria (BG)
      Byemite
    • Cyprus (CY)
    • Czechia (CZ)
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
许可日期2008/12/23
最近更新日期2021/03/24
药物ATC编码
    • QP53AF01 phoxime
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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