# Commission Regulation (EC) No 1836/97 of 24 September 1997 amending Annexes I 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 (Text with EEA relevance), 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.. Antiparasitic 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
‘2.3.1.4.
Doramectin
Doramectin
Porcine, ovine
20 μg/kg
Muscle
Not for use in ovines producing milk for human consumption’
100 μg/kg
Fat
50 μg/kg
Liver
30 μg/kg
Kidney
B.. Annex III is amended as follows:
2.. Antiparasitic agents
2.2. Agents acting against ectoparasites
2.2.1. Formamidines
Pharmacologically active substance
Marker residue
Animal species
MRLs
Target tissues
Other provisions
‘2.2.1.1.
Amitraz
Sum of amitraz and all metabolites containing the 2,4-dimethylaniline moiety, expressed as amitraz
Bees
200 μg/kg
Honey
Provisional MRLs expire on 1.7.1999’
2.2.2. Organophosphates
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target tissues
Other provisions
‘2.2.2.1.
Azamethiphos
Azamethiphos
Salmonidae
100 μg/kg
Muscle and skin in natural proportions Provisional
MRLs expire on 1. 6. 1999’

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Source: https://www.legislation.gov.uk/eur/1997/1836/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-1997-1836/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

