# Commission Regulation (EC) No 716/97 of 23 April 1997 amending Annexes II 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, Annex

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

Regulation (EEC) No 2377/90 is amended as follows:
A.. Annex II is modified as follows:
2.. Organic compounds
Pharmacologically active substance(s)
Animal species
Other provisions
‘2.85.
D-Phe6-Muteinizing-hormone-releasing-hormone
All food producing species
2.86.
Neostigmine
All food producing species’
B.. Annex III is modified as follows:
2.. Antiparasitic agents
2.3. Agents acting against endo- and ectoparasites
2.3.1. Avermectins
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
Other provisions
‘2.3.1.6.
Ivermectin
22,23-Dihydro-avermectin B 1 a
Deer, including reindeer
20 μg/kg
Muscle
Provisional MRLs expire on 1. 1. 1999’
100 μg/kg
Fat
50 μg/kg
Liver
20 μg/kg
Kidney

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Source: https://www.legislation.gov.uk/eur/1997/716/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-1997-716/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.