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Annex

United Kingdom

Original text. Later amendments are not shown.

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 SubstanceMarker residueAnimal SpeciesMRLTarget TissuesOther Provisions (according to Article 14(7) of Regulation (EC) No 470/2009)Therapeutic Classification
‘MonensinMonensin ABovine2 μg/kgMuscleNO ENTRYAnti-infectious agents/Antibiotics’
10 μg/kgFat
50 μg/kgLiver
10 μg/kgKidney
2 μg/kgMilk