Zeromectin 5 mg/ml Pour-on Solution for beef and dairy cattle
Zeromectin 5 mg/ml Pour-on Solution for beef and dairy cattle
Authorised
- Eprinomectin
Product identification
Medicine name:
Zeromectin 5 mg/ml Pour-on Solution for beef and dairy cattle
Zeromectin 5 mg/ml Pour-on Solution for beef and dairy cattle
Active substance:
- Eprinomectin
Target species:
-
Cattle
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
-
Meat and offal15day
-
Milk0hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- High density polyethylene container with a polypropylene tamper evident screw cap which consists of the following:5L 'Flexi' packs.
- High density polyethylene container with a polypropylene tamper evident screw cap which consists of the following:3L 'Flexi' packs.Pack sizes 3L
- High density polyethylene container with a polypropylene tamper evident screw cap which consists of the following:2.5 L 'Flexi' packs.Pack sizes 2.5L
- High density polyethylene container with a polypropylene tamper evident screw cap which consists of the following:1L 'Squeeze pour' packs.Pack sizes 1L
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10987/109/001
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0356/001
Concerned member states:
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet