Flukiver 50 mg/ml Solution for Injection
Flukiver 50 mg/ml Solution for Injection
Not authorised
- Closantel sodium
Product identification
Medicine name:
Flukiver 50 mg/ml Solution for Injection
Active substance:
- Closantel sodium
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Closantel sodium51.66/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal77day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AG09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Ireland
Available in:
-
Ireland
Package description:
- Container or pack size: 4 amber Type I glass vials. Closure: Grey bromobutyl siliconised rubber stopper. Cap: Aluminium cap with silver aluminium flip-off lid.Contents of each vial: 250 ml aqueous solution.
- Container or pack size: 1 amber Type I glass vial. Closure: Grey bromobutyl siliconised rubber stopper. Cap: Aluminium cap with silver aluminium flip-off lid.Contents of each vial: 250 ml aqueous solution.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
- Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Elanco France S.A.S
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA22020/002/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
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