VITAMIN A+D3+E, 50.000 i.j./25.000 i.j./10 mg, otopina za primjenu u vodi za piće, za goveda, ovce, koze, konje, svinje, kokoši, pse i mačke
VITAMIN A+D3+E, 50.000 i.j./25.000 i.j./10 mg, otopina za primjenu u vodi za piće, za goveda, ovce, koze, konje, svinje, kokoši, pse i mačke
Authorised
- ALPHATOCOPHEROL ACETATE
- Colecalciferol
- Retinol palmitate
Product identification
Medicine name:
VITAMIN A+D3+E, 50.000 i.j./25.000 i.j./10 mg, otopina za primjenu u vodi za piće, za goveda, ovce, koze, konje, svinje, kokoši, pse i mačke
Active substance:
- ALPHATOCOPHEROL ACETATE
- Colecalciferol
- Retinol palmitate
Target species:
-
Cattle
-
Sheep
-
Goat
-
Horse
-
Pig
-
Chicken
-
Dog
-
Cat
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
ALPHATOCOPHEROL ACETATE10.00/milligram(s)1.00millilitre(s)
-
Colecalciferol25000.00/international unit(s)1.00millilitre(s)
-
Retinol palmitate50000.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Cattle
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Goat
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Chicken
-
Eggs0day
-
-
Dog
-
Meat and offalno withdrawal periodN/A
-
-
Cat
-
Meat and offalno withdrawal periodN/A
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11JA
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Croatia
Package description:
- Available only in Croatian
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:
- Genera d.d.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/20-01/801
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
Croatian (PDF)
Published on: 11/02/2022