Veterinary Medicines

VITAMIN AD3E, emulzija za injekciju, goveda, ovce, koze, konji, svinje, kunići, psi, mačke

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

Medicine name:
VITAMIN AD3E, emulzija za injekciju, goveda, ovce, koze, konji, svinje, kunići, psi, mačke
Active substance:
  • DL-ALPHA-TOCOPHEROL
  • Colecalciferol
  • Retinol palmitate
Target species:
  • Cattle
  • Sheep
  • Goat
  • Horse
  • Pig
  • Rabbit
  • Dog
  • Cat
  • Cattle
  • Sheep
  • Goat
  • Horse
  • Pig
  • Rabbit
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • DL-ALPHA-TOCOPHEROL
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Colecalciferol
    25000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Retinol palmitate
    50000.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        243
        day
    • Sheep
      • Meat and offal
        187
        day
    • Goat
      • Meat and offal
        187
        day
    • Horse
      • Meat and offal
        243
        day
    • Pig
      • Meat and offal
        215
        day
    • Rabbit
      • Meat and offal
        122
        day
    • Dog
    • Cat
  • Subcutaneous use
    • Cattle
      • Meat and offal
        243
        day
    • Sheep
      • Meat and offal
        187
        day
    • Goat
      • Meat and offal
        187
        day
    • Horse
      • Meat and offal
        243
        day
    • Pig
      • Meat and offal
        215
        day
    • Rabbit
      • Meat and offal
        122
        day
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11JA
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
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 d.d. Novo Mesto
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/17-01/509
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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