Gallifen 40 mg/g premix for medicated feeding stuff for chickens and pheasants
Gallifen 40 mg/g premix for medicated feeding stuff for chickens and pheasants
Authorised
- Fenbendazole
Product identification
Medicine name:
Gallifen 40 mg/g premix for medicated feeding stuff for chickens and pheasants
ГАЛИФЕН 40 mg/g премикс за медикаментозен фураж за пилета и фазани
Active substance:
- Fenbendazole
Target species:
-
Chicken
-
Pheasant
Route of administration:
-
In-feed use
Product details
Active substance and strength:
-
Fenbendazole40.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Premix for medicated feeding stuff
Withdrawal period by route of administration:
-
In-feed use
-
Chicken
-
Eggs0day
-
Meat and offal8day
-
-
Pheasant
-
Eggs0day
-
Meat and offal8dayDo not release pheasants for hunting for at least 8 days after the end of medication
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AC13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- Polyethylene/aluminium foil/polyethylene terephthalate zipper bags of 5 kg.
- Polyethylene/aluminium foil/polyethylene terephthalate zipper bags of 2 kg.
- Polyethylene/aluminium foil/polyethylene terephthalate zipper bags of 1 kg.
- Polyethylene-aluminium-paper /paper/paper bag of 20 kg.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet AD
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2857
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0555/001
Concerned member states:
-
Belgium
-
Bulgaria
-
France
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 25/09/2024
Bulgarian (PDF)
Published on: 10/12/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 10/12/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 10/12/2024