Coglapix
Coglapix
Authorised
- Actinobacillus pleuropneumoniae, APX II toxoid
- Actinobacillus pleuropneumoniae, APX I toxoid
- Actinobacillus pleuropneumoniae, APX III toxoid
Product identification
Medicine name:
Coglapix
Coglapix suspensija injekcijām cūkām
Active substance:
- Actinobacillus pleuropneumoniae, APX II toxoid
- Actinobacillus pleuropneumoniae, APX I toxoid
- Actinobacillus pleuropneumoniae, APX III toxoid
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Actinobacillus pleuropneumoniae, APX II toxoid16.70enzyme-linked immunosorbent assay unit/millilitre2.00millilitre(s)
-
Actinobacillus pleuropneumoniae, APX I toxoid28.90enzyme-linked immunosorbent assay unit/millilitre2.00millilitre(s)
-
Actinobacillus pleuropneumoniae, APX III toxoid6.80enzyme-linked immunosorbent assay unit/millilitre2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- Cardboard box containing 5 vial of 100 ml
- Cardboard box containing 1 vial of 100 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva-Phylaxia Zrt.
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva-Phylaxia Veterinary Biologicals Co. Ltd.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/MRP/15/0041
Date of authorisation status change:
Reference member state:
-
Hungary
Procedure number:
- HU/V/120/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
Finland
-
Germany
-
Greece
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 18/01/2022
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 18/01/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 18/01/2022
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