Veterinary Medicines

Eprivalan 5mg/ml pour-on solution for cattle

Not authorised
  • Eprinomectin
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Product identification

Medicine name:
Eprivalan 5mg/ml pour-on solution for cattle
Eprivalan 5 mg/ml roztok na nalievanie na chrbát - pour-on pre mäsový a mliekový hovädzí dobytok
Active substance:
  • Eprinomectin
Target species:
  • Cattle
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
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Slovakia
Package description:
  • Back-pack (5 litre) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing device capable of delivering measured amounts of product. The 5 litre back-packs are designed for use with a suitable automatic dispensing gun.
  • Back-pack (2.5 litre) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing device capable of delivering measured amounts of product. The 2.5 litre back-packs are designed for use with a suitable automatic dispensing gun.
  • HDPE bottle (1 litre) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing device capable of delivering measured amounts of product. The 1 litre bottle uses a 50 ml dispenser (screw-on-squeeze-and-pour measuring chamber).
  • HDPE bottle (250 ml) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing device capable of delivering measured amounts of product. The 250 ml bottle uses a 25 ml dispenser (screw-on-squeeze-and-pour measuring chamber).

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:
  • Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/014/DC/17-S
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0487/001

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 2/02/2022
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Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
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