# Commission Regulation (EC) No 281/96 of 14 February 1996 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 (Text with EEA relevance), Annex Extent: E+W+S+N.I. A.. Annex I is amended as follows: 1.. Anti-infectious agents 1.1. Chemotherapeutics 1.1.1. Sulfonamides Pharmacologically active substance Marker residue Animal Species MRLs Target tissues Other provisions ‘All substances belonging to the sulfonamide group Parent drug Bovine Ovine Caprine 100 μg/kg Milk The combined residues of all substances in the sulfonamide group should not exceed 100 μg/kg’ 1.2. Antibiotics 1.2.6. Tetracylines Pharmacologically active substance Marker residue Animal Species MRLs Target Tissues Other provisions ‘1.2.6.1. Tetracycline Sum of parent drug and its 4-epimer All food producing species 600 μg/kg Kidney 300 μg/kg Liver 100 μg/kg Muscle 100 μg/kg Milk 200 μg/kg Eggs 1.2.6.2. Oxytetracycline Sum of parent drug and its 4-epimer All food producing species 600 μg/kg Kidney 300 μg/kg Liver 100 μg/kg Muscle 100 μg/kg Milk 200 μg/kg Eggs 1.2.6.3. Chlortetracycline Sum of parent drug and its 4-epimer All food producing species 600 μg/kg Kidney 300 μg/kg Liver 100 μg/kg Muscle 100 μg/kg Milk 200 μg/kg Eggs’ B.. Annex III is amended as follows: 1.. Anti-infectious agents 1.1. Chemotherapeutics 1.1.2. Diamino pyrimidine derivates Pharmacologically active substance(s) Marker residue Animal species MRLs Target tissues Other provisions ‘1.1.2.1. Trirnethoprim Trimethoprim All food producing species 50 μg/kg Muscle, liver, kidney, fat, milk Provisional MRLs expire on 1 January 1998’ --- Source: https://www.legislation.gov.uk/eur/1996/281/annex (the official version) Page: https://openlegislation.uk/eu-regulation-1996-281/annex Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.