Veterinary Medicines Information website

Bovipour 5 mg/ml pour-on solution for cattle

Authorised
  • Ivermectin
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Product identification

Medicine name:
Bovipour 5 mg/ml pour-on solution for cattle
Active substance:
  • Ivermectin
Target species:
  • Cattle
Route of administration:
  • Pour-on use

Product details

Active substance and strength:
  • Ivermectin
    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
        28
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
Package description:
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure (1 L).The 1 L pack will also have a dial a dose dosing cup.Pack sizes: 1 L.
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure (2.5 L).Pack sizes: 2.5 L.
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure (5 L).Pack sizes: 5 L.
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure.The 1 L pack will also have a dial a dose dosing cup.Pack sizes: 6 L.The 6L pack size consists of a 5 L and 1 L pack combined in one carton.
  • High density polyethylene squeeze measure pour containers with child resistantclosures. Pack sizes: 250 ml.
  • High density polyethylene squeeze measure pour containers with child resistantclosures. Pack sizes: 500 ml.
  • High density polyethylene squeeze measure pour containers with child resistantclosures. Pack sizes: 1 L.

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:
  • Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 1827 ESP
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0212/001
Concerned member states:
  • Austria
  • Spain

Documents

Summary of Product Characteristics

English (PDF)
Published on: 8/11/2026
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Spanish (PDF)
Published on: 14/03/2026
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 14/03/2026
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 14/03/2026
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Combined File of all Documents

English (PDF)
Published on: 8/11/2026
Download