Norbonex 5 mg/ml Pour-on Solution for Beef and Dairy Cattle
Norbonex 5 mg/ml Pour-on Solution for Beef and Dairy Cattle
Not authorised
- Eprinomectin
Product identification
Medicine name:
Norbonex 5 mg/ml Pour-on Solution for Beef and Dairy Cattle
Active substance:
- Eprinomectin
Target species:
-
Cattle (for meat production)
-
Cattle (dairy cow)
Route of administration:
-
Pour-on use
Product details
Active substance and strength:
-
Eprinomectin5.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Pour-on use
-
Cattle (for meat production)
-
Meat and offal10day
-
-
Cattle (dairy cow)
-
Meat and offal10day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
United Kingdom (Northern Ireland)
Package description:
- (ID5) 1 litre(s): unspecified outer container with 1 Barrel (Polyethylen hoher Dichte) with 1 litre(s)
- (ID4) 5 litre(s): unspecified outer container with 1 Barrel (Polyethylen hoher Dichte) with 5 litre(s)
- (ID3) 2.5 litre(s): unspecified outer container with 1 Barrel (Polyethylen hoher Dichte) with 2.5 litre(s)
- (ID2) 1 litre(s): unspecified outer container with 1 Container (Polyethylen hoher Dichte) with 1 litre(s), closed with Schnappdeckel (Polyethylen hoher Dichte)
- (ID1) 250 millilitre(s): unspecified outer container with 1 Container (Polyethylen hoher Dichte) with 250 millilitre(s), closed with Schnappdeckel (Polyethylen hoher Dichte)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Norbrook Laboratories Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories (Ireland) Limited
- Norbrook Laboratories Limited
Responsible authority:
- The Veterinary Medicines Directorate
Authorisation number:
- Vm 02000/4342
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0327/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet