Baycox Multi 50 mg/ml oral suspension for Cattle, Pigs and Sheep
Baycox Multi 50 mg/ml oral suspension for Cattle, Pigs and Sheep
Authorised
- Toltrazuril
Product identification
Medicine name:
Baycox Multi 50 mg/ml oral suspension for Cattle, Pigs and Sheep
Baycox Multi 50 mg/ml Suspensie voor oraal gebruik
Baycox Multi 50 mg/ml Suspension buvable
Baycox Multi 50 mg/ml Suspension zum Einnehmen
Active substance:
- Toltrazuril
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Toltrazuril50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal63day
-
-
Sheep
-
Meat and offal42day
-
-
Pig
-
Meat and offal77day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51BC01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- 100 ml high density polyethylene bottles closed with polypropylene screw caps.
- 250 ml high density polyethylene bottles closed with polypropylene screw caps.
- 1000 ml high density polyethylene bottles closed with polypropylene screw caps.
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-V504355
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0360/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
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
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Labelling
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Combined File of all Documents
English (PDF)
Download Published on: 6/07/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.