Veterinary Medicines

Paracox-8 vet. suspensjon til mikstur, suspensjon til kylling

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

Medicine name:
Paracox-8 vet. suspensjon til mikstur, suspensjon til kylling
Active substance:
  • Eimeria praecox, strain HP, Live
  • Eimeria necatrix, strain HP, Live
  • Eimeria acervulina, Live
  • Eimeria mitis, strain HP, Live
  • Eimeria maxima, strain CP, Live
  • Eimeria maxima, strain MFP, Live
  • Eimeria brunetti, strain HP, Live
  • Eimeria tenella, strain HP, Live
Target species:
  • Chicken
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Eimeria praecox, strain HP, Live
    100.00
    oocyst(s)
    /
    0.00
    millilitre(s)
  • Eimeria necatrix, strain HP, Live
    500.00
    oocyst(s)
    /
    0.00
    millilitre(s)
  • Eimeria acervulina, Live
    500.00
    oocyst(s)
    /
    0.00
    millilitre(s)
  • Eimeria mitis, strain HP, Live
    1000.00
    oocyst(s)
    /
    0.00
    millilitre(s)
  • Eimeria maxima, strain CP, Live
    200.00
    oocyst(s)
    /
    0.00
    millilitre(s)
  • Eimeria maxima, strain MFP, Live
    100.00
    oocyst(s)
    /
    0.00
    millilitre(s)
  • Eimeria brunetti, strain HP, Live
    100.00
    oocyst(s)
    /
    0.00
    millilitre(s)
  • Eimeria tenella, strain HP, Live
    500.00
    oocyst(s)
    /
    0.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Chicken
      • 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:
  • Norway
Package description:

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:
  • MSD Animal Health UK Limited
Responsible authority:
  • Norwegian Medical Products Agency
Authorisation number:
  • 0000-08234
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.
Norwegian (PDF)
Published on: 2/09/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Norwegian (PDF)
Published on: 2/09/2024
Download