Finadyne Transdermal 50 mg/ml pour-on solution for cattle
Finadyne Transdermal 50 mg/ml pour-on solution for cattle
Authorised
- Flunixin meglumine
Product identification
Medicine name:
Finadyne Transdermal 50 mg/ml pour-on solution for cattle
Finadyne transdermaal, 50 mg/ml pour-on oplossing voor runderen
Active substance:
- Flunixin meglumine
Target species:
-
Cattle
Route of administration:
-
Topical use
Product details
Active substance and strength:
-
Flunixin meglumine83.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Topical use
- Cattle
-
Meat and offal7day
-
Milk36hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AG90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- High density polyethylene (HDPE) bottles with polypropylene (PP) closures which have a peelable foil laminate induction innerseal and a liner. The bottles are equipped with a graduated dosing chamber and are supplied individually in a cardboard carton.Container size: 100 ml
- High density polyethylene (HDPE) bottles with polypropylene (PP) closures which have a peelable foil laminate induction innerseal and a liner. The bottles are equipped with a graduated dosing chamber and are supplied individually in a cardboard carton.Container size: 250 ml
- High density polyethylene (HDPE) bottles with polypropylene (PP) closures which have a peelable foil laminate induction innerseal and a liner. The bottles are equipped with a graduated dosing chamber and are supplied individually in a cardboard carton.Container size: 1000 ml
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:
- Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vet Pharma Friesoythe GmbH
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 113694
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0323/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 26/01/2022
Summary of Product Characteristics
English (PDF)
Download Published on: 11/02/2022
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