Veterinary Medicines

Colfive 5,000,000 IU/ml concentrate for oral solution for calves, pigs, lambs, chickens and turkeys

Not authorised
  • COLISTIN SULFATE
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Product identification

Medicine name:
COLFIVE 5.000.000 UI/ML
Colfive 5,000,000 IU/ml concentrate for oral solution for calves, pigs, lambs, chickens and turkeys
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:
  • Surrendered
Authorised in:
  • Ireland
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:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10425/001/001
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0221/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 22/12/2023
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Package Leaflet

English (PDF)
Published on: 22/12/2023
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Labelling

English (PDF)
Published on: 22/12/2023
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