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) 2018/722 of 16 May 2018 amending Regulation (EU) No 37/2010 to classify the substance eprinomectin as regards its maximum residue limit (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 ↗
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union . It shall apply from 16 July 2018.
ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘eprinomectin’ is replaced by the following: Pharmacologically active Substance Marker residue Animal Species MRLs Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic Classification ‘Eprinomectin Eprinomectin B1a All ruminants, equidae 50 μg/kg Muscle NO ENTRY Antiparasitic agents/Agents acting against endo- and ectoparasites’ 250 μg/kg Fat 1 500 μg/kg Liver 300 μg/kg Kidney 20 μg/kg Milk Fin fish 50 μg/kg Muscle and skin in natural proportions Rabbits 50 μg/kg Muscle 250 μg/kg Fat 1 500 μg/kg Liver 300 μg/kg Kidney
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