Annex
United Kingdom
In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance monensin 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 ‘Monensin Monensin A Bovine 2 μg/kg Muscle NO ENTRY Anti-infectious agents/Antibiotics’ 10 μg/kg Fat 50 μg/kg Liver 10 μg/kg Kidney 2 μg/kg Milk