# Commission Regulation (EC) No 748/97 of 25 April 1997 amending Annex I and II 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.

The Annexes to Regulation (EEC) No 2377/90 are amended as follows:
A.. Annex I is amended as follows:
2.. Anti-parasitic agents
2.3. Agents acting against endo- and ectoparasites
2.3.1. Avermectins
Pharmacologically active substance
Marker residue
Animal species
MRLs
Target tissues
Other provisions
‘2.3.1.5.
Moxidectin
Moxidectin
Bovine, ovine
500 μg/kg
Fat
100 μg/kg
Liver
50 μg/kg
Muscle, kidney’
B.. Annex II is amended as follows:
2.. Organic compounds
OJ No L 125, 23. 5. 1996, p. 3.’
Pharmacologically active substance(s)
Animal species
Other provisions
‘2.79.
Isoxsuprine
Bovine, equidae
For therapeutic use only in accordance with Council Directive 96/22/EEC
2.80.
Praziquantel
Ovine
For use in non-lactating sheep only

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Source: https://www.legislation.gov.uk/eur/1997/748/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-1997-748/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.