{
  "url": "https://openlegislation.uk/eu-regulation-2009-478/annex/division-2",
  "json_url": "https://openlegislation.uk/eu-regulation-2009-478/annex/division-2.json",
  "legislation": "eur/2009/478",
  "legislation_title": "Commission Regulation (EC) No 478/2009 of 8 June 2009 amending Annexes I and III to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards monepantel (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2009-478",
  "path": "annex/division/2",
  "kind": "division",
  "number": "(2)",
  "heading": "A new point 2.1.8 ‘Others’ which includes the new substance ‘Monepantel’ is added to Annex III (List of pharmacologically active substances used in veterinary medicinal products for which provisional maximum residue limits have been fixed), as follows:",
  "text": "2.\nAntiparasitic agents\n2.1.\nAgents acting against endoparasites\n‘2.1.8.\nOthers\nPharmacologically active substance(s)\nMarker residue\nAnimal species\nMRLs\nTarget tissues\nOther provisions\nMonepantel\nMonepantel-sulfone\nCaprine\n700 μg/kg\nMuscle\nNot for use in animals producing milk for human consumption\nProvisional maximum residue limit expires on 1 January 2011’\n7 000 μg/kg\nFat\n5 000 μg/kg\nLiver\n2 000 μg/kg\nKidney",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2009/478/annex/division/2",
    "retrieved_at": "2026-11-01T14:51:28.005771+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}