# Commission Regulation (EC) No 582/2009 of 3 July 2009 amending Annex I to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards diclofenac (Text with EEA relevance), Annex

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

In point 4.1.6 of Annex I (List of pharmacologically active substances for which maximum residue limits have been fixed) to Regulation (EEC) No 2377/90 the entry for ‘Diclofenac’ is replaced by the following:
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
‘Diclofenac
Diclofenac
Bovine
5 μg/kg
Muscle
1 μg/kg
Fat
5 μg/kg
Liver
10 μg/kg
Kidney
0,1 μg/kg
Milk
Porcine
5 μg/kg
Muscle
1 μg/kg
Skin + fat
5 μg/kg
Liver
10 μg/kg
Kidney’

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Source: https://www.legislation.gov.uk/eur/2009/582/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-2009-582/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.