Veterinary Medicines

Colfive 5,000,000 IU/ml solution for use in drinking water/milk for calves, pigs, lambs, chickens and turkeys

Authorised
  • COLISTIN SULFATE
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Product identification

Medicine name:
Colfive 5,000,000 IU/ml solution for use in drinking water/milk for calves, pigs, lambs, chickens and turkeys
Colfive 5 000 000 IU/ml koncentrát na perorálny roztok pre teľatá, ošípané, jahňatá, kurčatá a morky
Active substance:
  • COLISTIN SULFATE
Target species:
  • Pig
  • Turkey
  • Cattle (calf)
  • Sheep (lamb)
  • Chicken
Route of administration:
  • In drinking water/milk use
  • Oral use

Product details

Active substance and strength:
  • COLISTIN SULFATE
    5000000.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Concentrate for oral solution
Withdrawal period by route of administration:
  • In drinking water/milk use
    • Pig
      • Meat and offal
        1
        day
    • Turkey
      • Meat and offal
        1
        day
      • Eggs
        0
        day
    • Cattle (calf)
      • Meat and offal
        1
        day
    • Sheep (lamb)
      • Meat and offal
        1
        day
    • Chicken
      • Meat and offal
        1
        day
      • Eggs
        0
        day
  • Oral use
    • Pig
      • Meat and offal
        1
        day
    • Turkey
      • Meat and offal
        1
        day
      • Eggs
        0
        day
    • Cattle (calf)
      • Meat and offal
        1
        day
    • Sheep (lamb)
      • Meat and offal
        1
        day
    • Chicken
      • Meat and offal
        1
        day
      • Eggs
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07AA10
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:
  • bottle of 5 l
  • bottle of 1 l
  • box containing 1 bottle of 100 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Industrial Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Industrial Veterinaria S.A.
  • aniMedica GmbH
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/039/DC/15-S
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0221/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 24/07/2025
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Slovak (PDF)
Published on: 6/06/2023
Updated on: 8/06/2023
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Summary of Product Characteristics

English (PDF)
Published on: 20/10/2025
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Package Leaflet

English (PDF)
Published on: 20/10/2025
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Labelling

English (PDF)
Published on: 20/10/2025
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