Veterinary Medicines Information website

Eprecis 20 mg/ml solution for injection for cattle, sheep and goats

Authorised
  • Eprinomectin
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Product identification

Medicine name:
Eprecis 20 mg/ml solution for injection for cattle, sheep and goats
Active substance:
  • Eprinomectin
Target species:
  • Cattle
  • Goat
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Eprinomectin
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        63
        day
      • Milk
        0
        hour
    • Goat
      • Meat and offal
        42
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        42
        day
      • Milk
        0
        hour
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:
  • Nature of immediate packaging:Amber multilayer plastic vial (polypropylene / ethylene vinyl alcohol / polypropylene) with bromobutyl rubber stopper andaluminium cap and plastic flip-off disc in a cardboard box.Pack size: 50 ml vial
  • Nature of immediate packaging:Amber multilayer plastic vial (polypropylene / ethylene vinyl alcohol / polypropylene) with bromobutyl rubber stopper andaluminium cap and plastic flip-off disc in a cardboard box.Pack size: 100 ml vial
  • Nature of immediate packaging:Amber multilayer plastic vial (polypropylene / ethylene vinyl alcohol / polypropylene) with bromobutyl rubber stopper andaluminium cap and plastic flip-off disc in a cardboard box.Pack size: 250 ml vial
  • Nature of immediate packaging:Amber multilayer plastic vial (polypropylene / ethylene vinyl alcohol / polypropylene) with bromobutyl rubber stopper andaluminium cap and plastic flip-off disc in a cardboard box.Pack size: 500 ml vial

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:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V477511
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0340/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2026
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Dutch (PDF)
Published on: 13/03/2026
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French (PDF)
Published on: 13/03/2026
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German (PDF)
Published on: 13/03/2026
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 17/08/2025
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German (PDF)
Published on: 17/08/2025
Download
Dutch (PDF)
Published on: 13/03/2026
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 13/03/2026
Download
German (PDF)
Published on: 17/08/2025
Download
Dutch (PDF)
Published on: 13/03/2026
Download