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) 2015/2062 of 17 November 2015 amending Regulation (EU) No 37/2010 as regards the substance ‘sisapronil’ (Text with EEA relevance)
Commission Implementing Regulation (EU) 2015/2062 of 17 November 2015 amending Regulation (EU) No 37/2010 as regards the substance ‘sisapronil’ (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 twentieth day following that of its publication in the Official Journal of the European Union . It shall apply from 17 January 2016.
Supplementary provisions
ANNEXSupplementary provisions
ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, an entry for the following substance is inserted in alphabetical order: 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 ‘Sisapronil Sisapronil Bovine, caprine 100 μg/kg 2 000 μg/kg 200 μg/kg 100 μg/kg Muscle Fat Liver Kidney Not for use in animals from which milk is produced for human consumption Antiparasitic agents/Agents against ectoparasites’
Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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