PARACOX-8 SUSPENSION POUR SUSPENSION ORALE POUR POULES
PARACOX-8 SUSPENSION POUR SUSPENSION ORALE POUR POULES
Authorised
- Eimeria maxima, strain MFP, Live
- Eimeria mitis, strain HP, Live
- Eimeria acervulina, strain HP, Live
- Eimeria tenella, strain HP, Live
- Eimeria brunetti, strain HP, Live
- Eimeria necatrix, strain HP, Live
- Eimeria praecox, strain HP, Live
- Eimeria maxima, strain CP, Live
Product identification
Medicine name:
PARACOX-8 SUSPENSION POUR SUSPENSION ORALE POUR POULES
Active substance:
- Eimeria maxima, strain MFP, Live
- Eimeria mitis, strain HP, Live
- Eimeria acervulina, strain HP, Live
- Eimeria tenella, strain HP, Live
- Eimeria brunetti, strain HP, Live
- Eimeria necatrix, strain HP, Live
- Eimeria praecox, strain HP, Live
- Eimeria maxima, strain CP, Live
Target species:
-
Chicken (layer hen)
-
Chicken (for reproduction)
-
Chicken (broiler)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Eimeria maxima, strain MFP, Live1.00unit(s)1.00Dose
-
Eimeria mitis, strain HP, Live1.00unit(s)1.00Dose
-
Eimeria acervulina, strain HP, Live1.00unit(s)1.00Dose
-
Eimeria tenella, strain HP, Live1.00unit(s)1.00Dose
-
Eimeria brunetti, strain HP, Live1.00unit(s)1.00Dose
-
Eimeria necatrix, strain HP, Live1.00unit(s)1.00Dose
-
Eimeria praecox, strain HP, Live1.00unit(s)1.00Dose
-
Eimeria maxima, strain CP, Live1.00unit(s)1.00Dose
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Chicken (layer hen)
-
All relevant tissues0day
-
-
Chicken (for reproduction)
-
All relevant tissues0day
-
-
Chicken (broiler)
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AN01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
- Merck Sharp & Dohme Animal Health S.L.
- MSD Animal Health UK Limited
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/0067423 0/1996
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 22/07/2024
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 22/05/2024
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