# Commission Implementing Regulation (EU) No 676/2014 of 19 June 2014 amending Regulation (EU) No 37/2010, as regards the substance ‘triclabendazole’ (Text with EEA relevance), Annex

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

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘triclabendazole’ 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
‘Triclabendazole
Sum of the extractable residues that may be oxidised to ketotriclabendazole
All ruminants
225 μg/kg
100 μg/kg
250 μg/kg
150 μg/kg
10 μg/kg
Muscle
Fat
Liver
Kidney
Milk
NO ENTRY
Antiparasitic agents/Agents against endoparasites’

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Source: https://www.legislation.gov.uk/eur/2014/676/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-2014-676/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.