# Commission Regulation (EC) No 1191/98 of 9 June 1998 amending Annexes I and II 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.

A.. Annex I to Regulation (EEC) No 2377/90 is amended as follows:
1.. Anti-infectious agents
1.2. Antibiotics
1.2.8. Naphtalene-ringed ansamycin
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target issues
Other provisions
‘Rifaximin
Rifaximin
Bovine
60 μg/kg
Milk’
2.. Anti-parasitic agents
2.1. Agents acting against endoparasites
2.1.3. Benzimidazoles and pro-benzimidazoles
Pharmacologically active substance(s)
Marker residue
Animal species
MRLs
Target issues
Other provisions
‘Albendazole
Sum of albendazole sulphoxide, albendazole sulphone, and albendazole 2-amino sulphone, expressed as albendazole
Bovine, ovine
100 μg/kg
Muscle
100 μg/kg
Fat
1 000 μg/kg
Liver
500 μg/kg
Kidney
100 μg/kg
Milk’
B.. Annex II to Regulation (EEC) No 2377/90 is amended as follows:
2.. Organic compounds
Pharmacologically active substance(s)
Animal species
Other provisions
‘Benzalkonium chloride
All food producing species
For use as an excipient at concentrations up to 0,05 % only’
Corticotropin
All food producing species
Denaverine hydrochloride
Bovine
Ketamine
All food producing species

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Source: https://www.legislation.gov.uk/eur/1998/1191/annex (the official version)
Page: https://openlegislation.uk/eu-regulation-1998-1191/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.