Baycox Direct 25 mg/ml Lösung zum Eingeben über das Trinkwasser für Hühner und Puten
Baycox Direct 25 mg/ml Lösung zum Eingeben über das Trinkwasser für Hühner und Puten
Authorised
- Toltrazuril
Product identification
Medicine name:
Baycox Direct 25 mg/ml Lösung zum Eingeben über das Trinkwasser für Hühner und Puten
Baycox 25 mg/ml Oplossing voor gebruik in drinkwater
Baycox 25 mg/ml Solution pour administration dans l’eau de boisson
Baycox 25 mg/ml Lösung zum Eingeben über das Trinkwasser
Active substance:
- Toltrazuril
Target species:
-
Turkey (hen)
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Toltrazuril25.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Turkey (hen)
-
Meat and offal16day
-
- Chicken
-
Meat and offal16day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51BC01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- 100 ml (available in cartons of 1 x 100 ml) white HDPE bottles closed with light green polypropylene screw cap with a red tamper evident seal.
- 1000 ml white HDPE bottles closed with light green polypropylene screw cap with a red tamper evident seal.
- 5000 ml white HDPE canister with an aluminium sealing disc, closed with a black polyethylene screw cap and a yellow tamper evident seal.
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+Veterinär Produkte GmbH
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V478480
Date of authorisation status change:
Reference member state:
-
Austria
Procedure number:
- AT/V/0012/001
Concerned member states:
-
Belgium
-
France
-
Germany
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Portugal
-
United Kingdom (Northern Ireland)
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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