Multivitamin injection (15 000 j.m. + 1000 j.m. + 20 mg + 10 mg + 5 mg + 3 mg + 35 mg + 25 mg + 0,05 mg) /ml Roztwór do wstrzykiwań
Multivitamin injection (15 000 j.m. + 1000 j.m. + 20 mg + 10 mg + 5 mg + 3 mg + 35 mg + 25 mg + 0,05 mg) /ml Roztwór do wstrzykiwań
Not authorised
- Retinol
- Colecalciferol
- ALPHA-TOCOPHEROL
- Thiamine
- Pyridoxine hydrochloride
- Riboflavin
- Dexpanthenol
- Nicotinamide
- Cyanocobalamin
Product identification
Medicine name:
Multivitamin injection (15 000 j.m. + 1000 j.m. + 20 mg + 10 mg + 5 mg + 3 mg + 35 mg + 25 mg + 0,05 mg) /ml Roztwór do wstrzykiwań
Active substance:
- Retinol
- Colecalciferol
- ALPHA-TOCOPHEROL
- Thiamine
- Pyridoxine hydrochloride
- Riboflavin
- Dexpanthenol
- Nicotinamide
- Cyanocobalamin
Target species:
-
Cattle
-
Sheep
-
Goat
-
Horse
-
Cat
-
Dog
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Retinol
-
Colecalciferol
-
ALPHA-TOCOPHEROL
-
Thiamine
-
Pyridoxine hydrochloride
-
Riboflavin
-
Dexpanthenol
-
Nicotinamide
-
Cyanocobalamin50.00/microgram(s)1.00microgram(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11EX
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Scanvet Poland Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0735
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
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 18/08/2025
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 18/08/2025
Labelling
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 18/08/2025