# Commission Implementing Regulation (EU) No 122/2012 of 13 February 2012 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 methylprednisolone (Text with EEA relevance), Annex

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

The entry for methylprednisolone in Table 1 of the Annex to Regulation (EU) No 37/2010 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
‘Methylprednisolone
Methylprednisolone
Bovine
10 μg/kg
Muscle
Corticoides/Glucocorticoides’
10 μg/kg
Fat
10 μg/kg
Liver
10 μg/kg
Kidney
2 μg/kg
Milk

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Source: https://www.legislation.gov.uk/eur/2012/122/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-122/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.