Paracox-8 suspenzia na perorálnu suspenziu pre kurčatá
Paracox-8 suspenzia na perorálnu suspenziu pre kurčatá
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
Product identification
Medicine name:
Paracox-8 suspenzia na perorálnu suspenziu pre kurčatá
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
Route of administration:
-
In drinking water use
-
Nebulisation use
Product details
Active substance and strength:
-
Eimeria tenella, strain HP, Live500.00Organisms0.00millilitre(s)
-
Eimeria praecox, strain HP, Live100.00Organisms0.00millilitre(s)
-
Eimeria necatrix, strain HP, Live500.00Organisms0.00millilitre(s)
-
Eimeria mitis, strain HP, Live1000.00Organisms0.00millilitre(s)
-
Eimeria maxima, strain MFP, Live100.00Organisms0.00millilitre(s)
-
Eimeria maxima, strain CP, Live200.00Organisms0.00millilitre(s)
-
Eimeria brunetti, strain HP, Live100.00Organisms0.00millilitre(s)
-
Eimeria acervulina, strain HP, Live500.00Organisms0.00millilitre(s)
Pharmaceutical form:
-
Suspension for oral suspension
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken
-
All relevant tissues0dayzero days
-
-
-
Nebulisation use
-
Chicken
-
All relevant tissues0dayzero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AN01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
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.
Marketing authorisation date:
Manufacturing sites for batch release:
- MSD Animal Health UK Ltd
- MERCK SHARP & DOHME ANIMAL HEALTH, S.L.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/143/00-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 3/01/2025
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