RESFLOR 300/16.5 MG/ML SOLUTION FOR INJECTION FOR CATTLE
RESFLOR 300/16.5 MG/ML SOLUTION FOR INJECTION FOR CATTLE
Authorised
- Florfenicol
- Flunixin meglumine
Product identification
Medicine name:
RESFLOR 300/16.5 MG/ML SOLUTION FOR INJECTION FOR CATTLE
Resflor 300/16,5 mg/ml injekció szarvasmarhák részére A.U.V.
Active substance:
- Florfenicol
- Flunixin meglumine
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Florfenicol300.00milligram(s)1.00millilitre(s)
-
Flunixin meglumine27.40milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal46day
-
Milkno withdrawal periodNo withdrawal period
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01BA99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Package description:
- Carton box containing 250 mL vial
- Carton box containing 100 mL vial
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vet Pharma Friesoythe GmbH
Responsible authority:
- National Food Chain Safety Office
Authorisation number:
- 2220/X/07 MgSzH ÁTI
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0167/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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