VITAMIVEN COMPLEJO SOLUCION INYECTABLE
VITAMIVEN COMPLEJO SOLUCION INYECTABLE
Authorised
- RIBOFLAVIN SODIUM PHOSPHATE
- Retinol
- Nicotinamide
- VITAMIN B6
- Thiamine hydrochloride
- Colecalciferol
- Dexpanthenol
- DL-ALPHA TOCOPHEROL ACETATE
- Cyanocobalamin
Product identification
Medicine name:
VITAMIVEN COMPLEJO SOLUCION INYECTABLE
Active substance:
- RIBOFLAVIN SODIUM PHOSPHATE
- Retinol
- Nicotinamide
- VITAMIN B6
- Thiamine hydrochloride
- Colecalciferol
- Dexpanthenol
- DL-ALPHA TOCOPHEROL ACETATE
- Cyanocobalamin
Target species:
-
Cattle
-
Sheep
-
Goat
-
Horse
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
RIBOFLAVIN SODIUM PHOSPHATE4.00/milligram(s)1.00millilitre(s)
-
Retinol30000.00/international unit(s)1.00millilitre(s)
-
Nicotinamide50.00/milligram(s)1.00millilitre(s)
-
VITAMIN B620.00/milligram(s)1.00millilitre(s)
-
Thiamine hydrochloride25.00/milligram(s)1.00millilitre(s)
-
Colecalciferol10000.00/international unit(s)1.00millilitre(s)
-
Dexpanthenol25.00/milligram(s)1.00millilitre(s)
-
DL-ALPHA TOCOPHEROL ACETATE5.00/milligram(s)1.00millilitre(s)
-
Cyanocobalamin0.05/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal28day
-
Milk0day
-
-
Sheep
-
Meat and offal28day
-
Milk0day
-
-
Goat
-
Meat and offal28day
-
Milk0day
-
-
Horse
-
Meat and offal28day
-
Milk0day
-
-
Pig
-
Meat and offal28day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11BA
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Package description:
- Available only in Spanish
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:
- Laboratorios E Industrias Iven S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Maymo S.A.U.
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 3845 ESP
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 25/06/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 30/11/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 9/11/2022