Article 1
Open ↗The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Source
Commission Implementing Regulation (EU) 2016/1834 of 17 October 2016 amending Regulation (EU) No 37/2010 as regards the substance monepantel (Text with EEA relevance)
Commission Implementing Regulation (EU) 2016/1834 of 17 October 2016 amending Regulation (EU) No 37/2010 as regards the substance monepantel (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
Open ↗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 17 December 2016.
Supplementary provisions
ANNEXSupplementary provisions
Open ↗ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘monepantel’ 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 ‘Monepantel Monepantel sulfone Ovine, caprine 700 μg/kg Muscle NO ENTRY Antiparasitic agents/Agents (acting) against endoparasites’ 7 000 μg/kg Fat 5 000 μg/kg Liver 2 000 μg/kg Kidney 170 μg/kg Milk Bovine 300 μg/kg Muscle Not for use in animals producing milk for human consumption 7 000 μg/kg Fat 2 000 μg/kg Liver 1 000 μg/kg Kidney
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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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