Veterinary Medicines

ADE-vit, Injekční roztok

Authorised
  • Ergocalciferol
  • Retinyl propionate
  • ALPHATOCOPHEROL ACETATE
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Product identification

Medicine name:
ADE-vit, Injekční roztok
Active substance:
  • Ergocalciferol
  • Retinyl propionate
  • ALPHATOCOPHEROL ACETATE
Target species:
  • Cattle
  • Horse
  • Pig
  • Sheep
  • Goat
  • Dog
  • Rabbit
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Ergocalciferol
    100000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • Retinyl propionate
    100000.00
    international unit(s)
    /
    1.00
    millilitre(s)
  • ALPHATOCOPHEROL ACETATE
    30.00
    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
    • Horse
      • Meat and offal
        243
        day
      • Milk
        120
        hour
    • Pig
      • Meat and offal
        228
        day
    • Sheep
      • Meat and offal
        194
        day
      • Milk
        120
        hour
    • Goat
      • Meat and offal
        194
        day
      • Milk
        120
        hour
    • 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:
  • Czechia
Package description:

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:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/084/01-C
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.
Czech (PDF)
Published on: 26/10/2022
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Package Leaflet

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Czech (PDF)
Published on: 26/10/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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