Adedriol 80-40-20, oplossing voor injectie
Adedriol 80-40-20, oplossing voor injectie
Authorised
- Retinol palmitate
- Colecalciferol
- D ALPHA TOCOFERIL ACETATE
Product identification
Medicine name:
Adedriol 80-40-20, oplossing voor injectie
Active substance:
- Retinol palmitate
- Colecalciferol
- D ALPHA TOCOFERIL ACETATE
Target species:
-
Cattle
-
Sheep
-
Cattle (calf)
-
Horse
-
Pig
-
Pig (piglet)
-
Horse (foal)
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Retinol palmitate80000.00international unit(s)1.00millilitre(s)
-
Colecalciferol40000.00international unit(s)1.00millilitre(s)
-
D ALPHA TOCOFERIL ACETATE20.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Milk5day
-
Meat and offal234day
-
- Sheep
-
Milk5day
-
Meat and offal178day
-
- Cattle (calf)
-
Meat and offal234day
-
- Horse
-
Meat and offal224day
-
Milk5day
-
- Pig
- Pig (piglet)
-
Meat and offal224day
-
- Horse (foal)
-
Meat and offal224day
-
Milk5day
-
- Dog
-
Not applicableno withdrawal period
-
- Cat
-
Not applicableno withdrawal period
-
Not applicableno withdrawal period
-
-
Subcutaneous use
- Cattle
-
Milk5day
-
Meat and offal234day
-
- Sheep
-
Milk5day
-
Meat and offal178day
-
- Cattle (calf)
-
Meat and offal234day
-
- Horse
-
Meat and offal224day
-
- Pig
-
Meat and offal224day
-
- Pig (piglet)
-
Meat and offal224day
-
- Horse (foal)
-
Meat and offal224day
-
- Dog
- Cat
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:
- Available only in Dutch
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:
- Eurovet Animal Health B.V.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 1273
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 7/03/2023
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