欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FR/V/0298/001
药品名称DOXIPULVIS 500 mg/g oral powder for use in drinking water/milk replacer
活性成分
    • DOXYCYCLINE hyclate 577.1 mg/g
剂型Powder for use in drinking water/milk
上市许可持有人SP Veterinaria
参考成员国 - 产品名称France (FR)
DOXIPULVIS 500 MG/G POUDRE POUR ADMINISTRATION DANS L’EAU DE BOISSON / ALIMENTS D’ALLAITEMENT (14192)
互认成员国 - 产品名称
    • Germany (DE)
      DOXIPULVIS S.P.
    • United Kingdom (Northern Ireland) (XI)
      Doxipulvis S.P. 500 mg/g Oral Powder
    • Ireland (IE)
      DOXIPULVIS S.P. 500mg/g Oral Powder
    • Spain (ES)
      DOXIPULVIS S.P. 500 mg/g POLVO PARA ADMINISTRACIÓN EN AGUA DE BEBIDA O LACTOREEMPLAZANTE
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Poland (PL)
    • Hungary (HU)
    • Cyprus (CY)
    • Romania (RO)
    • Malta (MT)
许可日期2016/07/27
最近更新日期2024/11/29
药物ATC编码
    • QJ01AA02 doxycycline
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:Other Generic application Art 13.3 Dir 2001/82/EC
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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