Veterinary Medicines

KANAMICINA FP 250 mg/ml, soluție injectabilă pentru cai, bovine, oi, capre, porci, găini, câini și pisici

Authorised
  • Kanamycin
Download as PDF

Product identification

Medicine name:
KANAMICINA FP 250 mg/ml, soluție injectabilă pentru cai, bovine, oi, capre, porci, găini, câini și pisici
Active substance:
  • Kanamycin
Target species:
  • Cattle
  • Pig
  • Sheep
  • Goat
  • Chicken (hen)
  • Dog
  • Cat
  • Horse
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Kanamycin
    250.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        36
        hour
      • Meat and offal
        10
        day
    • Pig
      • Meat and offal
        10
        day
    • Sheep
      • Milk
        36
        hour
      • Meat and offal
        10
        day
    • Goat
      • Meat and offal
        10
        day
      • Milk
        36
        hour
    • Chicken (hen)
      • Meat and offal
        10
        day
    • Horse
      • Meat and offal
        10
        day
  • Subcutaneous use
    • Cattle
      • Milk
        36
        hour
      • Meat and offal
        10
        day
    • Pig
      • Meat and offal
        10
        day
    • Sheep
      • Milk
        36
        hour
      • Meat and offal
        10
        day
    • Goat
      • Meat and offal
        10
        day
      • Milk
        36
        hour
    • Chicken (hen)
      • Meat and offal
        10
        day
    • Horse
      • Meat and offal
        10
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01GB04
Legal status of supply:
This information is not available for this product.
Authorisation status:
  • Valid
Authorised in:
  • Romania
Available in:
  • Romania
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
  • Pasteur Filiala Filipesti S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pasteur Filiala Filipesti S.A.
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 150291
Date of authorisation status change:

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 20/11/2025
Download