Veterinary Medicine Information website

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

Authorised
  • Eprinomectin
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Product identification

Medicine name:
Pereprin 5 mg/ml pour on solution for cattle, sheep and goats
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:
  • Valid
Authorised in:
  • Greece
Package description:
  • White high-density polyethylene 5 L bottle closed with black screw closure made of polypropylene with a polyethylene-lined sealing disk (wadding) for induction sealing inside. One 5 L bottle per cardboard box together with a spigot cap.
  • White high-density polyethylene backpack bottles of 1 L closed with black screw closure made of polypropylene with a polyethylene-lined sealing disk (wadding) for induction sealing inside. One 1 L bottle per cardboard box together with a spigot cap and backpack strap.
  • White high-density polyethylene 250 ml bottle closed with black screw closure made of polypropylene with a polyethylene-lined sealing disk (wadding) for induction sealing inside. One 250 ml bottle per cardboard box together with a spigot cap.
  • White high-density polyethylene backpack bottles of 2.5 L closed with black screw closure made of polypropylene with a polyethylene-lined sealing disk (wadding) for induction sealing inside. One 2.5 L bottle per cardboard box together with a spigot cap and backpack strap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biovet AD
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 55304/05-05-2026/K-0263901
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0607/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)
Generic of: