Veterinary Medicines

Anisec 0.5 % w/v Pour-on Solution

Authorised
  • Ivermectin
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Product identification

Medicine name:
Anisec 0.5 % w/v Pour-on Solution
Iverpour 0.5 % w/v Pour-on oplossing
Iverpour 0.5 % w/v Solution pour pour-on
Iverpour 0.5 % w/v Lösung zum übergiessen
Active substance:
  • Ivermectin
Target species:
  • Cattle
Route of administration:
  • Topical 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:
  • Topical 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:
  • Belgium
Package description:
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure.Pack size: 1L. The 1L pack will also have a dial a dose dosing cup.
  • High density polyethylene squeeze measure pour containers with child resistantclosures. Pack size: 500ml.
  • High density polyethylene squeeze measure pour containers with child resistantclosures. Pack size: 250ml.
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure.Pack sizes: 6L.The 6L consists of a 5L and 1L pack combined in one carton. The 1L pack will also have a dial a dose dosing cup.
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure.Pack size: 5L.
  • High density polyethylene container (flat bottomed flexi packs) with a 38mm tamperevident closure.Pack size: 2.5L.
  • High density polyethylene squeeze measure pour containers with child resistantclosures. Pack size: 1L.

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V277234
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0169/001
Concerned member states:
  • Belgium
  • Denmark
  • Germany
  • Netherlands

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
Download
French (PDF)
Published on: 22/03/2022
Download
German (PDF)
Published on: 22/03/2022
Download
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