# Commission Regulation (EU) No 362/2011 of 13 April 2011 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 monepantel (Text with EEA relevance), Annex

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

The entry Monepantel in Table 1 of the Annex to Regulation (EU) No 37/2010 shall be 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
‘Monepantel
Monepantel-sulfone
Ovine
700 μg/kg
7 000 μg/kg
5 000 μg/kg
2 000 μg/kg
Muscle
Fat
Liver
Kidney
Not for use in animals producing milk for human consumption.
Antiparasitic agents/Agents acting against endoparasites
Caprine
700 μg/kg
7 000 μg/kg
5 000 μg/kg
2 000 μg/kg
Muscle
Fat
Liver
Kidney
Provisional MRLs shall expire on 1 January 2012.
Not for use in animals producing milk for human consumption.
Antiparasitic agents/Agents acting against endoparasites’

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Source: https://www.legislation.gov.uk/eur/2011/362/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-362/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.