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
Active substance:
- Florfenicol
- Flunixin meglumine
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Florfenicol300.00/milligram(s)1.00millilitre(s)
-
Flunixin meglumine27.40/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal46day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption. Do not use in pregnant animals which are intended to produce milk for human consumption within 2 months of expected parturition.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01BA99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Carton box containing 100 mL vial
- Carton box containing 250 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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V300991
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
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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Combined File of all Documents
English (PDF)
Download Published on: 14/03/2026