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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 corresponding to prednisolone 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
‘PrednisolonePrednisoloneBovine4 μg/kgMuscleNO ENTRYCorticoids/Glucocorticoids’
4 μg/kgFat
10 μg/kgLiver
10 μg/kgKidney
6 μg/kgMilk
Equidae 4 μg/kgMuscle
8 μg/kgFat
6 μg/kgLiver
15 μg/kgKidney