Veterinary Medicines

Vitamine AD3E 450.000 pro inj. oplossing voor injectie

Authorised
  • Colecalciferol
  • Vitamin A concentrate (oily form), synthetic
  • DL-ALPHA TOCOPHEROL ACETATE
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Product identification

Medicine name:
Vitamine AD3E 450.000 pro inj. oplossing voor injectie
Active substance:
  • Colecalciferol
  • Vitamin A concentrate (oily form), synthetic
  • DL-ALPHA TOCOPHEROL ACETATE
Target species:
  • Cattle (cow)
  • Goat (adult female)
  • Sheep
  • Cattle (calf)
  • Horse
  • Pig
  • Pig (piglet)
  • Horse (foal)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Colecalciferol
    100000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Vitamin A concentrate (oily form), synthetic
    300000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • DL-ALPHA TOCOPHEROL ACETATE
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle (cow)
      • Milk
        5
        day
      • Meat and offal
        259
        day
    • Goat (adult female)
      • Milk
        5
        day
      • Meat and offal
        194
        day
    • Sheep
      • Milk
        5
        day
      • Meat and offal
        194
        day
    • Cattle (calf)
      • Meat and offal
        259
        day
    • Horse
      • Meat and offal
        222
        day
    • Pig
      • Meat and offal
        231
        day
    • Pig (piglet)
      • Meat and offal
        231
        day
    • Horse (foal)
      • Meat and offal
        222
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11BA
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Bruine glazen injectieflacon (type II), afgesloten met butylrubberstop en aluminium felscapsule.12 x 100 ml flacons, in polystyreen buitenverpakking.
  • Bruine glazen injectieflacon (type II), afgesloten met butylrubberstop en aluminium felscapsule.12 x 100 ml flacons, in polystyreen buitenverpakking.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Alfasan Nederland B.V.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 3705
Date of authorisation status change:

Documents

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Dutch (PDF)
Published on: 12/07/2023
Updated on: 13/07/2023
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