# Commission Implementing Regulation (EU) No 221/2012 of 14 March 2012 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 closantel (Text with EEA relevance), Annex

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

The entry corresponding to closantel 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
‘Closantel
Closantel
Bovine
1 000 μg/kg
Muscle
Antiparasitic agents/Agents against endoparasites’
3 000 μg/kg
Fat
1 000 μg/kg
Liver
3 000 μg/kg
Kidney
Ovine
1 500 μg/kg
Muscle
2 000 μg/kg
Fat
1 500 μg/kg
Liver
5 000 μg/kg
Kidney
Bovine, Ovine
45 μg/kg
Milk
Provisional MRL shall expire on 1 January 2014

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Source: https://www.legislation.gov.uk/eur/2012/221/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-221/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.