Veterinary Medicines

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

Authorised
  • Eprinomectin
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Product identification

Medicine name:
Eprinex Multi 5 mg/ml pour-on solution for cattle, sheep and goats
Eprinex vet 5 mg/ml kertavaleluliuos naudoille, lampaille ja vuohille
Active substance:
  • Eprinomectin
Target species:
  • Cattle
  • Goat
  • Sheep
Route of administration:
  • Topical 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:
  • Topical 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:
  • Finland
Package description:
  • 5 L HDPE back packSealed foil and tamper evident HDPE screw cap with polypropylene liner5L back-pack with a dispensing capOne back-pack per cardboard box.The 5 litre back-packs are designed for use with a suitable automatic dispensing gun.
  • 2.5 HDPE back packSealed foil and tamper evident HDPE screw cap with polypropylene liner2.5L back-pack with a dispensing capOne bottle or one back-pack per cardboard box.The 2.5 litre back-packs are designed for use with a suitable automatic dispensing gun.
  • 1 L HDPE bottleSealed foil and tamper evident HDPE screw cap with polypropylene liner1L bottle with 2 measuring devices (1 of 60 ml for cattle, 1 of 25 ml for sheep/goat)One bottle per cardboard box.
  • 250 ml HDPE bottleSealed foil and tamper evident HDPE screw cap with polypropylene liner250 ml bottle with 2 measuring devices of 25 ml (1 for cattle, 1 for sheep/goat)One bottle per cardboard box.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Boehringer Ingelheim Animal Health Denmark A/S
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Finnish Medicines Agency
Authorisation number:
  • 36062
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0347/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
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Finnish (PDF)
Published on: 6/06/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Finnish (PDF)
Published on: 6/06/2023
Download
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