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

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance tildipirosin 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
‘Tildipirosin Tildipirosin Bovine, caprine 400 μg/kg Muscle Not for use in animals from which milk is produced for human consumption. Anti-infectious agents/Antibiotics’
200 μg/kg Fat
2 000 μg/kg Liver
3 000 μg/kg Kidney
Porcine 1 200 μg/kg Muscle 
800 μg/kg Skin and fat in natural proportions
5 000 μg/kg Liver
10 000 μg/kg Kidney
