BYEMITE 500 MG/ML CONCENTRATE FOR SPRAYING EMULSION FOR LAYING HENS
BYEMITE 500 MG/ML CONCENTRATE FOR SPRAYING EMULSION FOR LAYING HENS
Authorised
- Phoxim
Product identification
Medicine name:
BYEMITE 500 MG/ML CONCENTRATE FOR SPRAYING EMULSION FOR LAYING HENS
ByeMite 500 mg/ml Concentraat voor huidspray, emulsie
ByeMite 500 mg/ml Solution à diluer pour émulsion pour pulvérisation cutanée
ByeMite 500 mg/ml Konzentrat zur Herstellung eines Sprays zur Anwendung auf der Haut, Emulsion
Active substance:
- Phoxim
Target species:
-
Chicken (layer hen)
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Phoxim500.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Concentrate for spray emulsion
Withdrawal period by route of administration:
-
Cutaneous use
-
Chicken (layer hen)
-
Meat and offal25dayRemove eggs before treatment. Discard eggs laid during and on the same day after the treatment.
Meat and offal: 25 days after the second treatment. -
Eggs12hourRemove eggs before treatment. Discard eggs laid during and on the same day after the treatment.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AF01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Elanco Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V333837
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0196/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Finland
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Sweden
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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Labelling
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Package Leaflet and Labelling
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