Veterinary Medicines

Paracox 8 oral suspension

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, Live
  • Eimeria brunetti, strain HP, Live
  • Eimeria acervulina, Live
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Product identification

Medicine name:
Paracox 8 oral suspension
Paracox 8, Suspension zur Herstellung einer oralen Suspension für Hühner
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, Live
  • Eimeria brunetti, strain HP, Live
  • Eimeria acervulina, Live
Target species:
  • Chicken (chick)
Route of administration:
  • In drinking water use
  • In drinking water/milk use
  • Topical

Product details

Active substance and strength:
  • Eimeria tenella, strain HP, Live
    500.00
    cells
    /
    0.00
    millilitre(s)
  • Eimeria praecox, strain HP, Live
    100.00
    cells
    /
    0.00
    millilitre(s)
  • Eimeria necatrix, strain HP, Live
    500.00
    cells
    /
    0.00
    millilitre(s)
  • Eimeria mitis, strain HP, Live
    1000.00
    cells
    /
    0.00
    millilitre(s)
  • Eimeria maxima, strain MFP, Live
    200.00
    cells
    /
    0.00
    millilitre(s)
  • Eimeria maxima, Live
    200.00
    cells
    /
    0.00
    millilitre(s)
  • Eimeria brunetti, strain HP, Live
    100.00
    cells
    /
    0.00
    millilitre(s)
  • Eimeria acervulina, Live
    500.00
    cells
    /
    0.00
    millilitre(s)
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken (chick)
      • Meat and offal
        0
        day
      • Egg
        0
        day
  • In drinking water/milk use
    • Chicken (chick)
      • Meat and offal
        0
        day
      • Egg
        0
        day
  • Topical
    • Chicken (chick)
      • Meat and offal
        0
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AN
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Available in:
  • Austria
Package description:
  • (ID2): 1 Box with 1 Bottle (Polyethylenterephthalat Glycol-modifiziert) with 20 millilitre(s) (20 millilitre(s))
  • (ID4): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 500 millilitre(s) (500 millilitre(s))
  • (ID3): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 100 millilitre(s) (100 millilitre(s))
  • (ID1): 1 Box with 1 Bottle (Polyethylenterephthalat Glycol-modifiziert) with 4 millilitre(s) (4 millilitre(s))

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet Ges.m.b.H.
Marketing authorisation date:
Manufacturing sites for batch release:
  • MSD Animal Health UK Limited
  • Merck Sharp & Dohme Animal Health S.L.
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 8-20214
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0210/001
Concerned member states:
  • Austria

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
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German (PDF)
Published on: 17/09/2024
Updated on: 18/08/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 17/09/2024
Updated on: 18/08/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 17/09/2024
Updated on: 18/08/2025
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