Quinoflox 100 mg/ml solution for use in drinking water, chicken and rabbits
Quinoflox 100 mg/ml solution for use in drinking water, chicken and rabbits
Authorised
- Enrofloxacin
Product identification
Medicine name:
Quinoflox 100 mg/ml solution for use in drinking water, chicken and rabbits
Active substance:
- Enrofloxacin
Target species:
-
Rabbit
-
Chicken
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Enrofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
Oral use
-
Rabbit
-
Meat and offal2day
-
-
Chicken
-
Meat and offal4dayEggs: Do not use in birds producing eggs for human consumption
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- 1 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction.
- 4 X 5 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction
- 5 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction
- 12 X 1 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction
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:
- Global Vet Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- S P Veterinaria S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V400434
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0144/001
Concerned member states:
-
Belgium
-
France
-
Germany
-
Italy
-
Poland
-
Romania
-
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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Combined File of all Documents
English (PDF)
Download Published on: 28/07/2025
Updated on: 13/03/2026
Labelling
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