Veterinary Medicines

VITAMIN AD3EC oralna emulzija, za goveda, konje, svinje, ovce, koze, kuniće, nerčeve, činčile, kokoši, purane, golubove

Not authorised
  • Sodium ascorbate
  • DL-ALPHA-TOCOPHEROL
  • Colecalciferol
  • Retinol palmitate
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Product identification

Medicine name:
VITAMIN AD3EC oralna emulzija, za goveda, konje, svinje, ovce, koze, kuniće, nerčeve, činčile, kokoši, purane, golubove
Active substance:
  • Sodium ascorbate
  • DL-ALPHA-TOCOPHEROL
  • Colecalciferol
  • Retinol palmitate
Target species:
  • Cattle
  • Horse
  • Pig
  • Sheep
  • Goat
  • Rabbit
  • Mink
  • Chinchilla
  • Chicken
  • Turkey
  • Pigeon
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Sodium ascorbate
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • DL-ALPHA-TOCOPHEROL
    30.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Colecalciferol
    5000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Retinol palmitate
    50000.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral emulsion
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Rabbit
      • Meat and offal
        0
        day
    • Mink
      • Meat and offal
        0
        day
    • Chinchilla
      • Meat and offal
        0
        day
    • Chicken
      • Eggs
        0
        day
    • Turkey
      • Meat and offal
        0
        day
    • Pigeon
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11JA
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Revoked
Authorised in:
  • Croatia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Krka-Farma d.o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/20-01/603
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Croatian (PDF)
Published on: 10/02/2022
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