# Commission Regulation (EC) No 1805/2006 of 7 December 2006 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 thiamphenicol, fenvalerate and meloxicam (Text with EEA relevance), Division 4.1.4: Oxicam derivatives

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

Pharmacologically active Substance(s)
Marker residue
Animal species
MRLs
Target tissues
‘Meloxicam
Meloxicam
Porcine, equidae, rabbit
20 μg/kg
Muscle
65 μg/kg
Liver
65 μg/kg
Kidney
Bovine, caprine
20 μg/kg
Muscle
65 μg/kg
Liver
65 μg/kg
Kidney
15 μg/kg
Milk’

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Source: https://www.legislation.gov.uk/eur/2006/1805/annex/division/4/division/4.1/division/4.1.4 (the official version)
Page: https://openlegislation.uk/eu-regulation-2006-1805/annex/division-4/division-4.1/division-4.1.4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.