Veterinary Medicines

PARACOX-8 BG

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
Download as PDF

Product identification

Medicine name:
PARACOX-8 BG
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 (chick)
Route of administration:
  • In drinking water use
  • Nebulisation use

Product details

Active substance and strength:
  • Eimeria tenella, strain HP, Live
    500.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria praecox, strain HP, Live
    100.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria necatrix, strain HP, Live
    500.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria mitis, strain HP, Live
    1000.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria maxima, strain MFP, Live
    100.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria maxima, strain CP, Live
    200.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria brunetti, strain HP, Live
    100.00
    oocyst(s)
    /
    1.00
    Dose
  • Eimeria acervulina, strain HP, Live
    500.00
    oocyst(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Oral suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AN01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Bulgaria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 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.
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-2300
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.
Bulgarian (PDF)
Published on: 23/08/2024
Download

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 23/08/2024
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 23/08/2024
Download