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 1161/2012 of 7 December 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 fenbendazole Text with EEA relevance
Commission Implementing Regulation (EU) No 1161/2012 of 7 December 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 fenbendazole 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 that of its publication in the Official Journal of the European Union . It shall apply from 6 February 2013.
Supplementary provisions
ANNEXSupplementary provisions
ANNEX The entry corresponding to fenbendazole 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 ‘Fenbendazole Sum of extractable residues which may be oxidised to oxfendazole sulfone All food-producing species except fin fish 50 μg/kg Muscle For porcine and poultry species the fat MRL relates to “skin and fat in natural proportions” Antiparasitic agents/Agents against endoparasites’ 50 μg/kg Fat 500 μg/kg Liver 50 μg/kg Kidney 10 μg/kg Milk 1 300 μg/kg Eggs
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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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