# Commission Regulation (EC) No 2232/2004 of 23 December 2004 amending Annexes I, II and III 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 altrenogest, beclomethasone dipropionate, cloprostenol, r-cloprostenol, sorbitan sesquioleate and toltrazuril (Text with EEA relevance), Division 6.1: Progestagens

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

Only for zootechnical use and in accordance with the provisions of Directive 96/22/EC.
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
‘Altrenogest
Altrenogest
Porcine
1 μg/kg
Skin and fat
0,4 μg/kg
Liver
Equidae
1 μg/kg
Fat
0,9 μg/kg
Liver’

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Source: https://www.legislation.gov.uk/eur/2004/2232/annex/division/A/division/6/division/6.1 (the official version)
Page: https://openlegislation.uk/eu-regulation-2004-2232/annex/division-A/division-6/division-6.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.