- Latest available (Revised)
- Original (As adopted by EU)
Commission Regulation (EC) No 426/98 of 23 February 1998 amending Annexes I, II and 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 (Text with EEA relevance)
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This is the original version as it was originally adopted in the EU.
This legislation may since have been updated - see the latest available (revised) version
Annex I is modified as follows:
Antiparasitic agents
Agents acting against endoparasites
Benzimidazoles and pro-benzimidazoles
Pharmacologically active substance | Marker residue | Animal Species | MRLs | Target tissues | Other provisions |
---|---|---|---|---|---|
‘Triclabendazole | Sum of the extractable residues that may be oxidised to ketotriclabendazole | Bovine, ovine | 100 μg/kg | Muscle, liver, kidney | Not for use in animals producing milk for human consumption’ |
Annex II is modified as follows:
Organic compounds
Pharmacologically active substance(s) | Animal species | Other provisions |
---|---|---|
‘Isoflurane | Equidae | For use as anaesthetic only’ |
Annex III is modified as follows:
Antiparasitic agents
Agents acting against ectoparasites
Acyl urea derivates
Pharmacologically active substance(s) | Marker residue | Animal Species | MRLs | Target tissues | Other provisions |
‘Teflubenzuron | Teflubenzuron | Salmonidae | 500 μg/kg | Muscle and skin in natural proportions | Provisional MRLs expire on 1.7.1999’ |
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Original (As adopted by EU): The original version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.
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