# 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), Annex

Extent: E+W+S+N.I.

The entry corresponding to diclazuril in Table 1 of the Annex to Regulation (EU) No 37/2010 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
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

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Source: https://www.legislation.gov.uk/eur/2013/115/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-2013-115/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.