Vitesel Suspension for Injection
Vitesel Suspension for Injection
Not authorised
- Potassium selenate
- DL-ALPHA TOCOPHEROL ACETATE
Product identification
Medicine name:
Vitesel Suspension for Injection
Active substance:
- Potassium selenate
- DL-ALPHA TOCOPHEROL ACETATE
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Potassium selenate4.20milligram(s)1.00millilitre(s)
-
DL-ALPHA TOCOPHEROL ACETATE68.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal28day
-
- Sheep
-
Meat and offal28day
-
- Pig
-
Meat and offal28day
-
-
Subcutaneous use
- Cattle
-
Meat and offal28day
-
- Sheep
-
Meat and offal28day
-
- Pig
-
Meat and offal28day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11J
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Ireland
Package description:
- Vitesel is marketed in 50 ml Type II glass vials (amber) sealed with bromobutyl bungs (grey) and aluminium caps.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- HPRA
Authorisation number:
- VPA22664/034/001
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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