KARIFLOX 25 mg/ml oral solution for calves
KARIFLOX 25 mg/ml oral solution for calves
Authorised
- Enrofloxacin
Product identification
Medicine name:
KARIFLOX 25 mg/ml oral solution for calves
KARIFLOX 25 mg/ml SOLUCION ORAL PARA TERNEROS
Active substance:
- Enrofloxacin
Target species:
-
Cattle
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Enrofloxacin25.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal11day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Package description:
- Container Material:High density polyethylene bottlesContainer Closure:Polyethylene screw capContainer Colour:WhiteContainer Volume: 5 litreDosing Device:For all containers a 20 ml measuring device of polypropylene is included.
- Container Material:High density polyethylene bottlesContainer Closure:Polyethylene screw capContainer Colour:WhiteContainer Volume: 1 litreDosing Device:For all containers a 20 ml measuring device of polypropylene is included.
- Container Material:High density polyethylene bottlesContainer Closure:Polyethylene screw capContainer Colour:WhiteContainer Volume: 500 mlDosing Device:For all containers a 20 ml measuring device of polypropylene is included.
- Container Material:High density polyethylene bottlesContainer Closure:Polyethylene screw capContainer Colour:WhiteContainer Volume: 250 mlDosing Device:For all containers a 20 ml measuring device of polypropylene is included.
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:
- Laboratorios Karizoo S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Karizoo S.A.
Responsible authority:
- Spanish Agency For Medicines And Health Products
Authorisation number:
- 2029 ESP
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0217/002
Concerned member states:
-
France
-
Germany
-
Netherlands
-
Spain
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: 3/05/2024
Spanish (PDF)
Published on: 16/02/2023
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 16/02/2023
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 16/02/2023
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