Multivitamin Injection
Multivitamin Injection
Not authorised
- Dexpanthenol
- Nicotinamide
- Retinol palmitate
- Pyridoxine
- Colecalciferol
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
- TOCOPHERYL ACETATE
- VITAMIN B12
Product identification
Medicine name:
Multivitamin Injection
Active substance:
- Dexpanthenol
- Nicotinamide
- Retinol palmitate
- Pyridoxine
- Colecalciferol
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
- TOCOPHERYL ACETATE
- VITAMIN B12
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Dexpanthenol25.00milligram(s)1.00millilitre(s)
-
Nicotinamide35.00milligram(s)1.00millilitre(s)
-
Retinol palmitate15000.00international unit(s)1.00millilitre(s)
-
Pyridoxine3.00milligram(s)1.00millilitre(s)
-
Colecalciferol25.00microgram(s)1.00millilitre(s)
-
RIBOFLAVIN SODIUM PHOSPHATE6.35milligram(s)1.00millilitre(s)
-
Thiamine hydrochloride12.71milligram(s)1.00millilitre(s)
-
TOCOPHERYL ACETATE21.95milligram(s)1.00millilitre(s)
-
VITAMIN B1225.00microgram(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
-
-
Pig
-
Meat and offal28day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal28day
-
Milk0day
-
-
Sheep
-
Meat and offal28day
-
Milk0day
-
-
Pig
-
Meat and offal28day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11JA
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Ireland
Package description:
- 100 ml type II glass (amber) containers, sealed with nitryl rubber bungs and aluminium caps.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent application (Article 13c of Directive No 2001/82/EC)
Marketing authorisation holder:
- Chem-Pharm
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
Responsible authority:
- HPRA
Authorisation number:
- VPA10823/017/001
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
English (PDF)
Download Published on: 3/05/2024
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