Toltrazuril
Toltrazuril
Authorised
- Toltrazuril
Product identification
Medicine name:
Toltrazuril
Coccinox 25 mg/ml Oplossing voor gebruik in drinkwater
Coccinox 25 mg/ml Solution pour administration dans l'eau de boisson
Coccinox 25 mg/ml Lösung zum Eingeben über das Trinkwasser
Active substance:
- Toltrazuril
Target species:
-
Turkey
-
Chicken
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Toltrazuril25.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
Oral use
-
Turkey
-
Meat and offal16day
-
-
Chicken
-
Meat and offal16day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51AJ01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- 1 x 50 ml - Type III amber glass bottle of 50 ml closed with tamper-evident HDPE screw caps with ring and colourless LDPE syringe insert. Each bottle is individually packed in a cardboard box
- 1 x 10 ml - Type III amber glass bottle of 10 ml closed with tamper-evident HDPE screw caps with ring and colourless LDPE syringe insert. Each bottle is individually packed in a cardboard box
- 10 x 50 ml - Type III amber glass bottle of 50 ml closed with tamper-evident HDPE screw caps with ring and colourless LDPE syringe insert. Each bottle is individually packed in a cardboard box
- 10 x 10 ml - Type III amber glass bottles of 10 ml closed with tamper-evident HDPE screw caps with ring and colourless LDPE syringe insert. Each bottle is individually packed in a cardboard box
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:
- Avimedical B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- FLORIS VETERINAIRE PRODUCTEN B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V554195
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0272/001
Concerned member states:
-
Belgium
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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