# Commission Implementing Regulation (EU) No 406/2013 of 2 May 2013 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance prednisolone (Text with EEA relevance), Annex

Extent: E+W+S+N.I.

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry corresponding to prednisolone 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
‘Prednisolone
Prednisolone
Bovine
4 μg/kg
Muscle
NO ENTRY
Corticoids/Glucocorticoids’
4 μg/kg
Fat
10 μg/kg
Liver
10 μg/kg
Kidney
6 μg/kg
Milk
Equidae
4 μg/kg
Muscle
8 μg/kg
Fat
6 μg/kg
Liver
15 μg/kg
Kidney

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Source: https://www.legislation.gov.uk/eur/2013/406/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-2013-406/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.