VIRBAMEC Pour-On solution for cattle 5 mg/ml
VIRBAMEC Pour-On solution for cattle 5 mg/ml
Authorised
- Ivermectin
Product identification
Medicine name:
VIRBAMEC Pour-On solution for cattle 5 mg/ml
Virbamec Pour-On bovins 5 mg/ml Pour-on oplossing
Virbamec Pour-On bovins 5 mg/ml Solution pour pour-on
Virbamec Pour-On bovins 5 mg/ml Lösung zum übergiessen
Active substance:
- Ivermectin
Target species:
-
Cattle
Route of administration:
-
Pour-on use
Product details
Active substance and strength:
-
Ivermectin0.50/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Pour-on use
-
Cattle
-
Meat and offal28day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Size: 5.0 LContainer: Opaque high density polyethylene pack.Closure: Low density polyethylene seal fitted with a child resistant screw cap.Dosing device: made of polyproylene, to be used in conjunction with a dosing gun.
- Size: 2.5 LContainer: Opaque high density polyethylene pack.Closure: Low density polyethylene seal fitted with a child resistant screw cap.Dosing device: made of polyproylene, to be used in conjunction with a dosing gun.
- Size: 1000 mlContainer: Opaque high density polyethylene bottle.Closure: Low density polyethylene seal fitted with a child resistant screw cap.Dosing device: separate measuring chamber, made of polyproylene, capable of delivering doses of 10 to 25 ml at 5 mlintervals
- Size: 500 mlContainer: Opaque high density polyethylene bottle.Closure: Low density polyethylene seal fitted with a child resistant screw cap.Dosing device: separate measuring chamber, made of polyproylene, capable of delivering doses of 10 to 25 ml at 5 mlintervals.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent (abridged application) - Council Directive 81/851/EEC
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V275055
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0499/001
Concerned member states:
-
Belgium
-
France
-
Germany
-
Luxembourg
-
Portugal
-
Spain
-
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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