K-Flor 100 mg/ml Solution for Use in Drinking Water for Pigs
  • Florfenikols
  • Valid
Authorised in these countries:
  • Poland
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Product identification

Medicine name:
K-FLOR 100 mg/ml Solution for use in drinking water for pigs
K-Flor 100 mg/ml Solution for Use in Drinking Water for Pigs
Active substance and strength:
  • Florfenikols
    12064.00
    milligram(s)/millilitre
    /
    1.00
    milligram(s)/millilitre
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01BA90
Authorisation number:
  • Vm 31223/4003
Product identification number:
  • 678b42c4-52ed-4de1-a175-998bca89f90f
Permanent identification number:
  • 600000015453

Product details

Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
  • Solution for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Pig
      • Meat and offal
        5
        week

Availability

Package description:
  • Pack sizes: Bottle of 1L. Containers: White high-density polyethylene (HDPE) bottle Closures: HDPE screw cap with induction sealing.
  • Pack sizes: Barrel of 5L. Containers: White high-density polyethylene (HDPE) barrel Closures: HDPE screw cap with induction sealing.
  • Pack sizes: Bottle of 500 ml Containers: White high-density polyethylene (HDPE) bottle Closures: HDPE screw cap with induction sealing.
Manufacturing sites for batch release:
  • Laboratorios Karizoo S.A.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • PL/V/0103/001
Date of authorisation status change:
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Authorisation country:
  • United Kingdom (Northern Ireland)
Responsible authority:
  • VMD
Marketing authorisation holder:
  • Laboratorios Karizoo S.A.
Marketing authorisation issued:
Reference member state:
  • Poland
Concerned member states:
  • Hungary
  • Portugal
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Summary of Product Characteristics (PDF)
First published:
Last updated:
Package Leaflet and Labelling (PDF)
First published:
Last updated:
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