Unomec 5 mg/ml Pour-on Solution for beef and dairy cattle
Unomec 5 mg/ml Pour-on Solution for beef and dairy cattle
Authorised
- Eprinomectin
Product identification
Medicine name:
Unomec 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:
-
Belgium
Package description:
- High density polyethylene container with a polypropylene tamper evident screw cap which consists of the following:1L 'Squeeze pour' packs.Pack sizes 1L.
- 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:3L 'Flexi' packs.Pack sizes 3L.
- High density polyethylene container with a polypropylene tamper evident screw cap which consists of the following:5L 'Flexi' packs.Pack sizes 5 L.
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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V519395
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0354/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Czechia
-
Denmark
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Combined File of all Documents
English (PDF)
Download Published on: 12/04/2026
Labelling
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