VITBPLEX Solution for Injection
VITBPLEX Solution for Injection
Not authorised
- Nicotinamide
- Ascorbic acid
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
- Pyridoxine hydrochloride
Product identification
Medicine name:
VITBPLEX Solution for Injection
Active substance:
- Nicotinamide
- Ascorbic acid
- RIBOFLAVIN SODIUM PHOSPHATE
- Thiamine hydrochloride
- Pyridoxine hydrochloride
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Nicotinamide23.00/milligram(s)1.00millilitre(s)
-
Ascorbic acid70.00/milligram(s)1.00millilitre(s)
-
RIBOFLAVIN SODIUM PHOSPHATE0.50/milligram(s)1.00millilitre(s)
-
Thiamine hydrochloride35.00/milligram(s)1.00millilitre(s)
-
Pyridoxine hydrochloride7.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11E
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Ireland
Package description:
- The veterinary medicinal product is packaged in a 100 ml amber Type II glass vial, sealed with bromobutyl bung and aluminium cap.
- The veterinary medicinal product is packaged in a 50 ml amber Type II glass vial, sealed with bromobutyl bung and aluminium cap.
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:
- VPA10823/018/001
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