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 1390/2014 of 19 December 2014 amending the Annex to Regulation (EU) No 37/2010, as regards the substance ‘eprinomectin’ Text with EEA relevance
Commission Implementing Regulation (EU) No 1390/2014 of 19 December 2014 amending the Annex to Regulation (EU) No 37/2010, as regards the substance ‘eprinomectin’ 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 22 February 2015.
Supplementary provisions
ANNEXSupplementary provisions
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 MRL Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic classification ‘Eprinomectin Eprinomectin B1a Bovine 50 μg/kg 250 μg/kg 1 500 μg/kg 300 μg/kg 20 μg/kg Muscle Fat Liver Kidney Milk NO ENTRY Antiparasitic agents/Agents acting against endo- and ectoparasites’ Ovine, caprine 50 μg/kg 250 μg/kg 1 500 μg/kg 300 μg/kg 20 μg/kg Muscle Fat Liver Kidney Milk Provisional maximum residue limits expire on 30 June 2016
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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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