Paracox-8, zawiesina do sporządzania zawiesiny doustnej dla kur
Paracox-8, zawiesina do sporządzania zawiesiny doustnej dla kur
Authorised
- Eimeria praecox, strain HP, Live
- Eimeria tenella, strain HP, Live
- Eimeria necatrix, strain HP, Live
- Eimeria brunetti, strain HP, Live
- Eimeria tenella, strain HP, Live
- Eimeria mitis, strain HP, Live
- Eimeria maxima, strain CP, Live
- Eimeria acervulina, strain HP, Live
Product identification
Medicine name:
Paracox-8, zawiesina do sporządzania zawiesiny doustnej dla kur
Active substance:
- Eimeria praecox, strain HP, Live
- Eimeria tenella, strain HP, Live
- Eimeria necatrix, strain HP, Live
- Eimeria brunetti, strain HP, Live
- Eimeria tenella, strain HP, Live
- Eimeria mitis, strain HP, Live
- Eimeria maxima, strain CP, Live
- Eimeria acervulina, strain HP, Live
Target species:
-
Chicken (hen)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Eimeria praecox, strain HP, Live650.00unknown1.00unknown
-
Eimeria tenella, strain HP, Live130.00unknown1.00unknown
-
Eimeria necatrix, strain HP, Live650.00unknown1.00unknown
-
Eimeria brunetti, strain HP, Live1300.00unknown1.00unknown
-
Eimeria tenella, strain HP, Live130.00unknown1.00unknown
-
Eimeria mitis, strain HP, Live260.00unknown1.00unknown
-
Eimeria maxima, strain CP, Live130.00unknown1.00unknown
-
Eimeria acervulina, strain HP, Live650.00unknown1.00unknown
Pharmaceutical form:
-
Suspension for oral suspension
Withdrawal period by route of administration:
-
Oral use
- Chicken (hen)
-
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:
-
Poland
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:
- Merck Sharp & Dohme Animal Health S.L.
- Merck Sharp & Dohme Animal Health S.L.
- MSD Animal Health UK Limited
- MSD Animal Health UK Limited
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0988
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.
Polish (PDF)
Published on: 26/01/2024
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 29/01/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 29/01/2024
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