Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats
Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats
Authorised
- Eprinomectin
Product identification
Medicine name:
Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats
EPRECIS 5 MG/ML SOLUTION POUR POUR-ON POUR BOVINS, OVINS ET CAPRINS
Active substance:
- Eprinomectin
Target species:
-
Cattle
-
Goat
-
Sheep
Route of administration:
-
Pour-on use
Product details
Active substance and strength:
-
Eprinomectin5.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Pour-on use
-
Cattle
-
Meat and offal15day
-
Milk0hour
-
-
Goat
-
Meat and offal1day
-
Milk0hour
-
-
Sheep
-
Meat and offal2day
-
Milk0hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Available in:
-
France
Package description:
- *HISTORICAL* Squeeze-measure pour-on system:250 ml translucent high density polyethylene (HDPE) bottle including 10 ml dispenser graduated each 5 ml, with removablealuminium/PE seals and PE screw cap.
- Back pack:1 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap or 1 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap included in acardboard box.
- Back pack:2.5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap or 2.5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap included in acardboard box.
- Back pack:5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap or 5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap included in acardboard box.
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:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/1482427 6/2015
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0343/001
Concerned member states:
-
Belgium
-
Denmark
-
France
-
Germany
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
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: 30/03/2025
French (PDF)
Published on: 7/04/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 7/04/2025
Combined File of all Documents
English (PDF)
Download Published on: 30/03/2025
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