Norocillin 300 mg/ml Suspension for Injection
Norocillin 300 mg/ml Suspension for Injection
Authorised
- Benzylpenicillin procaine
Product identification
Medicine name:
Norocillin 300 mg/ml Suspension for Injection
Active substance:
- Benzylpenicillin procaine
Target species:
-
Cattle
-
Sheep
-
Horse
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Benzylpenicillin procaine300.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal5dayFor treatment duration 3-5 days.
-
Meat and offal7dayFor treatment duration 6-7 days.
-
Milk96hour
-
-
Sheep
-
Meat and offal5dayFor treatment duration 3-5 days.
-
Meat and offal7dayFor treatment duration 6-7 days.
-
-
Horse
-
Meat and offal28dayFor treatment duration of 3-5 days.
-
Meat and offal30dayFor treatment duration 6-7 days.
-
-
Pig
-
Meat and offal5dayFor treatment duration 3-5 days.
-
Meat and offal7dayFor treatment duration 6-7 days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CE01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Available in:
-
Ireland
Package description:
- 250 ml multidose clear polyethylene terephthalate (PET) vials closed with bromobutyl rubber bungs and aluminium caps.
- 100 ml multidose type II clear glass vials closed with bromobutyl rubber bungs and aluminium caps.
- 50 ml multidose clear polyethylene terephthalate (PET) vials closed with bromobutyl rubber bungs and aluminium caps.
- 100 ml multidose clear polyethylene terephthalate (PET) vials closed with bromobutyl rubber bungs and aluminium caps.
- 50 ml multidose type II clear glass vials closed with bromobutyl rubber bungs and aluminium caps.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA22664/012/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
