Veterinary Medicines

Hipracox Broilers Spray

Not authorised
  • Eimeria acervulina, strain 003, Live
  • Eimeria maxima, strain 013, Live
  • Eimeria mitis, strain 006, Live
  • Eimeria praecox, strain 007, Live
  • Eimeria tenella, strain 004, Live
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Product identification

Medicine name:
Hipracox Broilers Spray
HIPRACOX Suspensão e solução para spray para frangos.
Active substance:
  • Eimeria acervulina, strain 003, Live
  • Eimeria maxima, strain 013, Live
  • Eimeria mitis, strain 006, Live
  • Eimeria praecox, strain 007, Live
  • Eimeria tenella, strain 004, Live
Target species:
  • Chicken (broiler)
Route of administration:
  • Nebulisation use

Product details

Active substance and strength:
  • Eimeria acervulina, strain 003, Live
    390.00
    Organisms
    /
    1.00
    Dose
  • Eimeria maxima, strain 013, Live
    260.00
    Organisms
    /
    1.00
    Dose
  • Eimeria mitis, strain 006, Live
    390.00
    Organisms
    /
    1.00
    Dose
  • Eimeria praecox, strain 007, Live
    390.00
    Organisms
    /
    1.00
    Dose
  • Eimeria tenella, strain 004, Live
    325.00
    Organisms
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension and solution for spray
Withdrawal period by route of administration:
  • Nebulisation use
    • Chicken (broiler)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AN01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Revoked
Authorised in:
  • Portugal
Package description:
  • cardboard box containing 10 vials of 5000 doses (100 ml)
  • cardboard box containing 6 vials of 5000 doses (100 ml)
  • cardboard box containing 5 vials of 5000 doses (100 ml)
  • cardboard box containing 1 vial of 5000 doses (100 ml)
  • cardboard box containing 10 vials of 1000 doses (20 ml)
  • cardboard box containing 1 vial of 1000 doses (20 ml)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • LABORATORIOS HIPRA, S.A.
  • The Veterinary Medicines Directorate
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 792/08 RIVPT
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0327/001