VECOXAN 2.5 MG/ML ORAL SUSPENSION
VECOXAN 2.5 MG/ML ORAL SUSPENSION
Authorised
- Diclazuril
Product identification
Medicine name:
VECOXAN 2.5 MG/ML ORAL SUSPENSION
Vecoxan 2,5 mg/ml belsőleges szuszpenzió bárányoknak és borjaknak
Active substance:
- Diclazuril
Target species:
-
Cattle (calf)
-
Sheep (lamb)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Diclazuril2.50/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cattle (calf)
-
Meat and offal0day
-
-
Sheep (lamb)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51BC03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Available in:
-
Hungary
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Productions S.A.
Responsible authority:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
- 2178/X/07 MgSzH ÁTI
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0113/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Portugal
-
Slovakia
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet