Veterinary Medicines

Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats

Not authorised
  • Eprinomectin
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Product identification

Medicine name:
Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats
Eprecis 5 mg/ml pour-on oplossing voor runderen, schapen en geiten
Active substance:
  • Eprinomectin
Target species:
  • Cattle
  • Goat
  • Sheep
Route of administration:
  • Pour-on use

Product details

Active substance and strength:
  • Eprinomectin
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Pour-on solution
Withdrawal period by route of administration:
  • Pour-on use
    • Cattle
      • Meat and offal
        15
        day
      • Milk
        0
        hour
    • Goat
      • Meat and offal
        1
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        2
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Netherlands
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 B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 115710
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0343/001

Documents

Combined File of all Documents

English (PDF)
Published on: 30/03/2025
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Dutch (PDF)
Published on: 26/01/2022
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Summary of Product Characteristics

English (PDF)
Published on: 30/03/2025
Download