# Commission Regulation (EC) No 1451/2006 of 29 September 2006 amending Annexes I and II 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 fluazuron, sodium nitrite and peforelin (Text with EEA relevance), Division 2.2.4: Acyl urea derivatives

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

Not for use in animals from which milk is produced for human consumption.’
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
‘Fluazuron
Fluazuron
Bovine
200 μg/kg
Muscle
7 000 μg/kg
Fat
500 μg/kg
Liver
500 μg/kg
Kidney

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Source: https://www.legislation.gov.uk/eur/2006/1451/annex/division/A/division/2/division/2.2/division/2.2.4 (the official version)
Page: https://openlegislation.uk/eu-regulation-2006-1451/annex/division-A/division-2/division-2.2/division-2.2.4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.