# Commission Regulation (EC) No 1323/2007 of 12 November 2007 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 firocoxib (Text with EEA relevance), Division 4.1.7

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

Sulphonated fenyl lactones
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
‘Firocoxib
Firocoxib
Equidae
10 μg/kg
Muscle
15 μg/kg
Fat
60 μg/kg
Liver
10 μg/kg
Kidney’

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Source: https://www.legislation.gov.uk/eur/2007/1323/annex/division/4/division/4.1/division/4.1.7 (the official version)
Page: https://openlegislation.uk/eu-regulation-2007-1323/annex/division-4/division-4.1/division-4.1.7
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.