PARACOX-5, SUSPENSION FOR ORAL SUSPENSION FOR CHICKENS
PARACOX-5, SUSPENSION FOR ORAL SUSPENSION FOR CHICKENS
Authorised
- Eimeria acervulina, strain HP, Live
- Carminic acid
- Eimeria maxima, strain CP, Live
- Eimeria tenella, strain HP, Live
- Eimeria mitis, strain HP, Live
- Eimeria maxima, strain MFP, Live
Product identification
Medicine name:
PARACOX-5, SUSPENSION FOR ORAL SUSPENSION FOR CHICKENS
Paracox-5 Suspensie voor suspensie voor oraal gebruik
Paracox-5 Suspension pour suspension buvable
Paracox-5 Suspension zur Herstellung einer Suspension zum Einnehmen
Active substance:
- Eimeria acervulina, strain HP, Live
- Carminic acid
- Eimeria maxima, strain CP, Live
- Eimeria tenella, strain HP, Live
- Eimeria mitis, strain HP, Live
- Eimeria maxima, strain MFP, Live
Target species:
-
Chicken (broiler)
-
Chicken (one day-old chick)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Eimeria acervulina, strain HP, Live500.00Organisms1.00Dose
-
Carminic acid0.10millilitre(s)1.00Dose
-
Eimeria maxima, strain CP, Live500.00Organisms1.00Dose
-
Eimeria tenella, strain HP, Live1000.00Organisms1.00Dose
-
Eimeria mitis, strain HP, Live100.00Organisms1.00Dose
-
Eimeria maxima, strain MFP, Live200.00Organisms1.00Dose
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
- Chicken (broiler)
-
All relevant tissues0day
-
- Chicken (one day-old chick)
-
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:
-
Belgium
Package description:
- Container of 5 plastic vials of 20 mL (5000 doses)
- Container of 1 plastic vial of 100 mL (1000 doses)
- Container of 1 plastic vial of 500 mL (5000 doses)
- Container of 5 plastic vials of 4 mL (1000 doses)
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:
- Merck Sharp & Dohme Animal Health S.L.
- MSD Animal Health UK Limited
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V211321
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0351/001
Concerned member states:
-
Austria
-
Belgium
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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