Virbamec Super Solution For Injection
Virbamec Super Solution For Injection
Authorised
- Ivermectin
- Clorsulon
Product identification
Medicine name:
Virbamec Super Solution For Injection
Virbamec F 10 mg/ml Oplossing voor injectie
Virbamec F 10 mg/ml Solution injectable
Virbamec F 10 mg/ml Injektionslösung
Active substance:
- Ivermectin
- Clorsulon
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin10.00/milligram(s)1.00millilitre(s)
-
Clorsulon100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal66day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- [Created in error/pack size deleted] Size 50 ml colourless LDPE vial with plastic overcap covering rubber stopper and aluminium overseal.
- Size 200 ml colourless LDPE vial with plastic overcap covering rubber stopper and aluminium overseal.
- Size 500 ml colourless LDPE vial with plastic overcap covering rubber stopper and aluminium overseal.
- Size 1000 ml colourless LDPE vial with plastic overcap covering rubber stopper and aluminium overseal.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
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-V274951
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0595/001
Concerned member states:
-
Belgium
-
France
-
Italy
-
Netherlands
-
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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