Flukiver Combi 50 mg/ml + 75 mg/ml oral suspension
Flukiver Combi 50 mg/ml + 75 mg/ml oral suspension
Authorised
- Mebendazole
- Closantel sodium dihydrate
Product identification
Medicine name:
Flukiver Combi 50 mg/ml + 75 mg/ml oral suspension
Active substance:
- Mebendazole
- Closantel sodium dihydrate
Target species:
-
Sheep
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Mebendazole75.00/milligram(s)1.00millilitre(s)
-
Closantel sodium dihydrate54.37/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Sheep
-
Meat and offal65day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52A
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Container: High density polyethylene bottles of 1 litre Closure: High density polyethylene screw cap
- Container: High density polyethylene bottles of 2.5 litresClosure: High density polyethylene screw cap
- Container: High density polyethylene bottles of 5 litresClosure: High density polyethylene screw cap
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 GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Lusomedicamenta Sociedade Tecnica Farmaceutica S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V344531
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0222/001
Concerned member states:
-
Austria
-
Belgium
-
France
-
Germany
-
Iceland
-
Italy
-
Netherlands
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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