Veterinary Medicines

PARACOX, suspenzija za peroralnu primjenu, kokoši

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

Product identification

Medicine name:
PARACOX, suspenzija za peroralnu primjenu, kokoši
Active substance:
  • Eimeria acervulina, strain HP, Live
  • Eimeria brunetti, strain HP, Live
  • Eimeria maxima, strain CP, Live
  • Eimeria maxima, strain MFP, Live
  • Eimeria mitis, strain HP, Live
  • Eimeria necatrix, strain HP, Live
  • Eimeria praecox, strain HP, Live
  • Eimeria tenella, strain HP, Live
Target species:
  • Chicken
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Eimeria acervulina, strain HP, Live
    500.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria brunetti, strain HP, Live
    100.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria maxima, strain CP, Live
    200.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria maxima, strain MFP, Live
    100.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria mitis, strain HP, Live
    1000.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria necatrix, strain HP, Live
    500.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria praecox, strain HP, Live
    100.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria tenella, strain HP, Live
    500.00
    oocyst(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Chicken
      • 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:
  • Valid
Authorised in:
  • Croatia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet International B.V. Subsidiary In The Republic Of Croatia
Marketing authorisation date:
Manufacturing sites for batch release:
  • Schering-Plough Limited
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/12-01/369
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.
Croatian (PDF)
Published on: 18/02/2022
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."