# 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 3.2.1

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

β 2 sympathomimetic agents
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
Other provisions
Clenbuterol hydrochloride
Clenbuterol
Bovine
0,1 μg/kg
Muscle
Provisional MRLs expire on 1 July 2000
Indication: solely for tocolysis in parturient cows
0,5 μg/kg
Liver
0,5 μg/kg
Kidney
0,05 μg/kg
Milk
Equidae
0,1 μg/kg
Muscle
Indications: tocolysis and the treatment of respiratory ailments
0,5 μg/kg
Liver
0,5 μg/kg
Kidney

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Source: https://www.legislation.gov.uk/eur/1999/508/annex/III/division/3/division/3.2/division/3.2.1 (the official version)
Page: https://openlegislation.uk/eu-regulation-1999-508/annex-III/division-3/division-3.2/division-3.2.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.