Article 1
Open ↗The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Source
Commission Implementing Regulation (EU) No 1235/2013 of 2 December 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
Commission Implementing Regulation (EU) No 1235/2013 of 2 December 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
Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
Article 2
Open ↗This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union . It shall apply from 3 February 2014.
Supplementary provisions
ANNEXSupplementary provisions
Open ↗ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for diclazuril is replaced by the following: Pharmacologically active Substance Marker residue Animal Species MRL Target Tissues Other Provisions ( according to Article 14(7) of Regulation (EC) No 470/2009 ) Therapeutic Classification ‘Diclazuril NOT APPLICABLE All ruminants, porcine No MRL required NOT APPLICABLE For oral use only NO ENTRY Diclazuril Poultry 500 μg/kg Muscle Not for use in animals from which eggs are produced for human consumption Antiparasitic agents/Agents acting againsts protozoa’ 500 μg/kg Skin and fat in natural proportions 1 500 μg/kg Liver 1 000 μg/kg Kidney Rabbit 150 μg/kg Muscle 300 μg/kg Fat 2 500 μg/kg Liver 1 000 μg/kg Kidney
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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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