LANFLOX 100 mg/ml Solution for use in drinking water for Chickens and Turkeys
LANFLOX 100 mg/ml Solution for use in drinking water for Chickens and Turkeys
Authorised
- Enrofloxacin
Product identification
Medicine name:
LANFLOX 100 mg/ml Solution for use in drinking water for Chickens and Turkeys
LANFLOX 100 MG/ML SOLUTION POUR UTILISATION DANS L'EAU DE BOISSON POUR POULETS ET DINDES
Active substance:
- Enrofloxacin
Target species:
-
Turkey
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Enrofloxacin100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Meat and offal13day
-
Eggno withdrawal period
-
-
Chicken
-
Eggno withdrawal period
-
Meat and offal7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- (ID3) 5 litre(s): unspecified outer container with 1 Barrel (High Density PolyEthylene) with 5 litre(s)
- (ID2) 1 litre(s): unspecified outer container with 1 Bottle (High Density PolyEthylene) with 1 litre(s)
- (ID1) 250 millilitre(s): unspecified outer container with 1 Bottle (High Density PolyEthylene) with 250 millilitre(s)
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:
- Vetpharma Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Karizoo S.A.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/6576746 9/2008
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0346/001
Concerned member states:
-
Belgium
-
France
-
Hungary
-
Ireland
-
Netherlands
-
Romania
-
United Kingdom (Northern Ireland)
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: 28/01/2022
French (PDF)
Published on: 27/06/2024
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 11/09/2024
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