Skip to main content
Veterinary Medicines

Paracox 8 suspenzija za peroralno suspenzijo za piščance

Authorised
  • Eimeria tenella, strain HP, Live
  • Eimeria praecox, strain HP, Live
  • Eimeria necatrix, strain HP, Live
  • Eimeria mitis, strain HP, Live
  • Eimeria maxima, strain MFP, Live
  • Eimeria maxima, strain CP, Live
  • Eimeria brunetti, strain HP, Live
  • Eimeria acervulina, strain HP, Live

Product identification

Medicine name:
Paracox 8 suspenzija za peroralno suspenzijo za piščance
Active substance:
  • Eimeria tenella, strain HP, Live
  • Eimeria praecox, strain HP, Live
  • Eimeria necatrix, strain HP, Live
  • Eimeria mitis, strain HP, Live
  • Eimeria maxima, strain MFP, Live
  • Eimeria maxima, strain CP, Live
  • Eimeria brunetti, strain HP, Live
  • Eimeria acervulina, strain HP, Live
Target species:
  • Chicken
Route of administration:
  • In-feed use
  • In drinking water use

Product details

Active substance and strength:
  • Eimeria tenella, strain HP, Live
    500.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria praecox, strain HP, Live
    100.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria necatrix, strain HP, Live
    500.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria mitis, strain HP, Live
    1000.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria maxima, strain MFP, Live
    100.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria maxima, strain CP, Live
    200.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria brunetti, strain HP, Live
    100.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria acervulina, strain HP, Live
    500.00
    Organisms
    /
    0.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for oral suspension
Withdrawal period by route of administration:
  • In-feed use
    • Chicken
      • Meat and offal
        0
        day
  • In drinking water use
    • Chicken
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AN01
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • MSD Animal Health UK Limited
  • Merck Sharp & Dohme Animal Health S.L.
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • NP/V/0252/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 17/09/2025

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 17/09/2025

Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 17/09/2025