# Commission Regulation (EC) No 508/1999 of 4 March 1999 amending Annexes I to IV 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, Division 4.1.2

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

Fenamate group derivatives
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
Other provisions
Tolfenamic acid
Tolfenamic acid
Bovine
50 μg/kg
Muscle
400 μg/kg
Liver
100 μg/kg
Kidney
50 μg/kg
Milk
Porcine
50 μg/kg
Muscle
400 μg/kg
Liver
100 μg/kg
Kidney

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Source: https://www.legislation.gov.uk/eur/1999/508/annex/I/division/4/division/4.1/division/4.1.2 (the official version)
Page: https://openlegislation.uk/eu-regulation-1999-508/annex-I/division-4/division-4.1/division-4.1.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.