
Article 1 
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
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.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 19 December 2014.
For the Commission
The President
Jean-Claude JUNCKER
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/kg250 μg/kg1 500 μg/kg300 μg/kg20 μg/kg MuscleFatLiverKidneyMilk NO ENTRY Antiparasitic agents/Agents acting against endo- and ectoparasites’
Ovine, caprine 50 μg/kg250 μg/kg1 500 μg/kg300 μg/kg20 μg/kg MuscleFatLiverKidneyMilk Provisional maximum residue limits expire on 30 June 2016
