# Commission Regulation (EC) No 1312/96 of 8 July 1996 amending Annex III of 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, Annex

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

A.. Annex III is modified as follows:
3.. Agents acting on the nervous system
3.2. Agents acting on the autonomic nervous system
3.2.2. β2 sympathomimetic agents
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
Other provisions
‘3.2.2.1.
Clenbuterol hydrochloride
Clenbuterol
Bovine
0,5 μg/kg
Liver, kidney
Provisional MRLs expire on 1.7.2000
0,1 μg/kg
Muscle
Indication: Solely for tocolysis in parturient cows
0,05 μg/kg
Milk
Equine
0,5 μg/kg
Liver, kidney
Provisional MRLs expire on 1.7.2000
0,1 μg/kg
Muscle
Indications: Tocolysis and the treatment of respiratory ailments’

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Source: https://www.legislation.gov.uk/eur/1996/1312/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-1996-1312/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.