{
  "url": "https://openlegislation.uk/eu-regulation-2013-115/annex",
  "json_url": "https://openlegislation.uk/eu-regulation-2013-115/annex.json",
  "legislation": "eur/2013/115",
  "legislation_title": "Commission Implementing Regulation (EU) No 115/2013 of 8 February 2013 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2013-115",
  "path": "annex",
  "kind": "annex",
  "number": null,
  "heading": null,
  "text": "The entry corresponding to diclazuril in Table 1 of the Annex to Regulation (EU) No 37/2010 is replaced by the following:\nPharmacologically active Substance\nMarker residue\nAnimal Species\nMRL\nTarget Tissues\nOther Provisions (according to Article 14(7) of Regulation (EC) No 470/2009)\nTherapeutic Classification\n‘Diclazuril\nNOT APPLICABLE\nAll ruminants, porcine\nNo MRL required\nNOT APPLICABLE\nFor oral use only\nNO ENTRY\nPoultry\n500 μg/kg\nMuscle\nNot for use in animals from which eggs are produced for human consumption\nAntiparasitic agents/Agents acting againsts protozoa’\n500 μg/kg\nSkin and fat in natural proportions\n1 500 μg/kg\nLiver\n1 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/2013/115/annex",
    "retrieved_at": "2026-11-01T14:48:51.882725+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."
}