Vitol-Ject Forte, oplossing voor injectie
Vitol-Ject Forte, oplossing voor injectie
Not authorised
- Ascorbic acid
- Nicotinamide
- Pyridoxine hydrochloride
- DL-ALPHA TOCOPHEROL ACETATE
- Dexpanthenol
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
- Cyanocobalamin
- Colecalciferol
- Retinyl propionate
Product identification
Medicine name:
Vitol-Ject Forte, oplossing voor injectie
Active substance:
- Ascorbic acid
- Nicotinamide
- Pyridoxine hydrochloride
- DL-ALPHA TOCOPHEROL ACETATE
- Dexpanthenol
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
- Cyanocobalamin
- Colecalciferol
- Retinyl propionate
Target species:
-
Cattle
-
Sheep
-
Cattle (calf)
-
Horse
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Ascorbic acid2.00milligram(s)1.00millilitre(s)
-
Nicotinamide12.50milligram(s)1.00millilitre(s)
-
Pyridoxine hydrochloride1.25milligram(s)1.00millilitre(s)
-
DL-ALPHA TOCOPHEROL ACETATE4.00milligram(s)1.00millilitre(s)
-
Dexpanthenol3.00milligram(s)1.00millilitre(s)
-
RIBOFLAVIN SODIUM PHOSPHATE2.00milligram(s)1.00millilitre(s)
-
Thiamine hydrochloride2.50milligram(s)1.00millilitre(s)
-
Cyanocobalamin3.00microgram(s)1.00millilitre(s)
-
Colecalciferol25000.00international unit(s)1.00millilitre(s)
-
Retinyl propionate50000.00international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milkno withdrawal period0 days
-
Meat and offalno withdrawal period0 days
-
-
Sheep
-
Milkno withdrawal period0 days
-
Meat and offalno withdrawal period0 days
-
-
Cattle (calf)
-
Meat and offalno withdrawal period0 days
-
-
Horse
-
Meat and offalno withdrawal period0 days
-
-
Pig
-
Meat and offalno withdrawal period0 days
-
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11BA
Legal status of supply:
-
Medicinal product not subject to medical prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Netherlands
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma B.V.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 4142
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: 22/02/2022
How useful was this page?: