# Commission Regulation (EC) No 1299/2005 of 8 August 2005 amending Annexes I 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 phenoxymethylpenicillin, phoxim, norgestomet and thiamphenicol (Text with EEA relevance), Division 6.1: Progestagens

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

For therapeutic and zootechnical purposes only.’
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
‘Norgestomet
Norgestomet
Bovine
0,2 μg/kg
Muscle
0,2 μg/kg
Fat
0,2 μg/kg
Liver
0,2 μg/kg
Kidney
0,12 μg/kg
Milk

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Source: https://www.legislation.gov.uk/eur/2005/1299/annex/division/A/division/6/division/6.1 (the official version)
Page: https://openlegislation.uk/eu-regulation-2005-1299/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.