PARACOX 8
PARACOX 8
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
Product identification
Medicine name:
PARACOX 8
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:
-
In drinking water use
-
Nebulisation use
-
Nebulisation use
Product details
Active substance and strength:
-
Eimeria acervulina, strain HP, Live500.00Organisms1.00Dose
-
Eimeria brunetti, strain HP, Live100.00Organisms1.00Dose
-
Eimeria maxima, strain CP, Live200.00Organisms1.00Dose
-
Eimeria maxima, strain MFP, Live100.00Organisms1.00Dose
-
Eimeria mitis, strain HP, Live1000.00Organisms1.00Dose
-
Eimeria necatrix, strain HP, Live500.00Organisms1.00Dose
-
Eimeria praecox, strain HP, Live100.00Organisms1.00Dose
-
Eimeria tenella, strain HP, Live500.00Organisms1.00Dose
Pharmaceutical form:
-
Suspension for oral suspension
Withdrawal period by route of administration:
-
In drinking water use
- Chicken
-
Meat and offal0day
-
-
Nebulisation use
- Chicken
-
Meat and offal0day
-
-
Nebulisation use
- Chicken
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AN01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Merck Sharp & Dohme Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- MSD Animal Health UK Limited
- Merck Sharp & Dohme Animal Health S.L.
Responsible authority:
- The Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 1660 ESP
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Labelling
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 15/12/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 15/12/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 15/12/2023
How useful was this page?: