Veterinary Medicines

Vitamine A + D3 + E Drank

Authorised
  • Cholecalciferol concentrate (powder form)
  • Retinol
  • ALPHATOCOPHEROL ACETATE
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Product identification

Medicine name:
Vitamine A + D3 + E Drank
Vitamine A + D3 + E Solution buvable
Vitamine A + D3 + E Lösung zum Einnehmen
Active substance:
  • Cholecalciferol concentrate (powder form)
  • Retinol
  • ALPHATOCOPHEROL ACETATE
Target species:
  • Pig
  • Cattle
  • Horse
  • Sheep
  • Goat
  • Chicken
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Cholecalciferol concentrate (powder form)
    25000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Retinol
    50000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • ALPHATOCOPHEROL ACETATE
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral solution
Withdrawal period by route of administration:
  • Oral use
    • Pig
      • Meat and offal
        28
        day
    • Cattle
      • Meat and offal
        28
        day
      • Milk
        no withdrawal period
    • Horse
      • Meat and offal
        28
        day
      • Milk
        no withdrawal period
    • Sheep
      • Meat and offal
        28
        day
      • Milk
        no withdrawal period
    • Goat
      • Meat and offal
        28
        day
      • Milk
        no withdrawal period
    • Chicken
      • Meat and offal
        28
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11BA
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Vitamine A + D3 + E 1 Bottle with 1 l of Oral solution
  • Vitamine A + D3 + E 1 Bottle with 500 ml of Oral solution
  • Vitamine A + D3 + E 1 Bottle with 250 ml of Oral solution
  • Vitamine A + D3 + E 1 Bottle with 100 ml of Oral solution

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
  • VMD N.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V102365
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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