Veterinary Medicines Information website

TRIAVIT injekčný roztok

Authorised
  • Retinol palmitate
  • CHOLECALCIFEROL CONCENTRATE
  • alfa-Tocopheryl acetate
Download as PDF

Product identification

Medicine name:
TRIAVIT injekčný roztok
Active substance:
  • Retinol palmitate
  • CHOLECALCIFEROL CONCENTRATE
  • alfa-Tocopheryl acetate
Target species:
  • Cattle
  • Pig
  • Horse
  • Sheep (lamb)
  • Chicken (for reproduction)
  • Rabbit
  • Dog
  • Ornamental bird
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Retinol palmitate
    100000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • CHOLECALCIFEROL CONCENTRATE
    50000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • alfa-Tocopheryl acetate
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        243
        day
      • Milk
        120
        hour
    • Pig
      • Meat and offal
        228
        day
    • Horse
      • Meat and offal
        243
        day
    • Sheep (lamb)
      • Meat and offal
        194
        day
    • Chicken (for reproduction)
      • Meat and offal
        56
        day
    • Rabbit
      • Meat and offal
        56
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11JA
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Pharmagal spol. s r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pharmagal spol. s r.o.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/006/01-S
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.
Slovak (PDF)
Published on: 26/01/2022
Download