
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 3 February 2014.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 2 December 2013.
For the Commission
The President
José Manuel BARROSO
ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for diclazuril 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
‘Diclazuril NOT APPLICABLE All ruminants, porcine No MRL required NOT APPLICABLE For oral use only NO ENTRY
Diclazuril Poultry 500 μg/kg Muscle Not for use in animals from which eggs are produced for human consumption Antiparasitic agents/Agents acting againsts protozoa’
500 μg/kg Skin and fat in natural proportions
1 500 μg/kg Liver
1 000 μg/kg Kidney
Rabbit 150 μg/kg Muscle 
300 μg/kg Fat
2 500 μg/kg Liver
1 000 μg/kg Kidney
