Article 1
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Commission Implementing Regulation (EU) No 222/2012 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 triclabendazole Text with EEA relevance
Commission Implementing Regulation (EU) No 222/2012 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 triclabendazole 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
This Regulation shall enter into force on the third day following its publication in the Official Journal of the European Union . It shall apply from 14 May 2012.
Supplementary provisions
ANNEXSupplementary provisions
ANNEX The entry corresponding to triclabendazole 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 ‘Triclabendazole Sum of the extractable residues that may be oxidised to ketotriclabendazole All ruminants 225 μg/kg Muscle Antiparasitic agents/agents against endoparasites’ 100 μg/kg Fat 250 μg/kg Liver 150 μg/kg Kidney 10 μg/kg Milk Provisional MRL shall expire on 1 January 2014
Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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