Veterinary Medicines

PARACOX-5, SUSPENSION FOR ORAL SUSPENSION FOR CHICKENS

Authorised
  • Eimeria maxima, strain CP, Live
  • Eimeria tenella, strain HP, Live
  • Eimeria mitis, strain HP, Live
  • Eimeria maxima, strain MFP, Live
  • Eimeria acervulina, strain HP, Live
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Product identification

Medicine name:
PARACOX-5, SUSPENSION FOR ORAL SUSPENSION FOR CHICKENS
Paracox 5 suspenzija za peroralno suspenzijo za piščance
Active substance:
  • Eimeria maxima, strain CP, Live
  • Eimeria tenella, strain HP, Live
  • Eimeria mitis, strain HP, Live
  • Eimeria maxima, strain MFP, Live
  • Eimeria acervulina, strain HP, Live
Target species:
  • Chicken (broiler)
  • Chicken (one day-old chick)
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Eimeria maxima, strain CP, Live
    500.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria tenella, strain HP, Live
    1000.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria mitis, strain HP, Live
    100.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria maxima, strain MFP, Live
    200.00
    Organisms
    /
    0.00
    millilitre(s)
  • Eimeria acervulina, strain HP, Live
    500.00
    Organisms
    /
    0.00
    millilitre(s)
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Chicken (broiler)
      • All relevant tissues
        0
        day
    • Chicken (one day-old chick)
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AN01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
Package description:
  • box of 5 vials of 4 mL (1000 doses)
  • 1 vial of 500 mL (solvent)
  • 1 vial of 100 mL (solvent)
  • box of 5 vials of 20 mL (5000 doses)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Merck Sharp & Dohme Animal Health S.L.
  • MSD Animal Health UK Limited
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • MR/V/0251/001
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0351/001
Concerned member states:
  • Austria
  • Belgium
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

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: 20/09/2024
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Package Leaflet

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Slovenian (PDF)
Published on: 20/09/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 20/09/2024
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