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Annex

United Kingdom

Original text. Later amendments are not shown.

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘tulathromycin’ is replaced by the following:

Pharmacologically active SubstanceMarker residueAnimal SpeciesMRLTarget TissuesOther Provisions (according to Article 14(7) of Regulation (EC) No 470/2009)Therapeutic classification
‘Tulathromycin(2R,3S,4R,5R,8R,10R,11R,12S, 13S,14R)-2-ethyl-3,4,10,13-tetra-hydroxy-3,5,8,10,12,14-hexamethyl-11-[[3,4,6-trideoxy-3-(dimethy-lamino)-ß-D-xylo-hexopyranosyl]oxy]-1-oxa-6-azacyclopent-decan-15-one expressed as tulathromycin equivalentsOvine, caprine450 μg/kgMuscleNot for use in animals from which milk is produced for human consumptionAnti-infectious agents/Antibiotics’
250 μg/kgFat
5 400 μg/kgLiver
1 800 μg/kgKidney
Bovine300 μg/kgMuscle
200 μg/kgFat
4 500 μg/kgLiver
3 000 μg/kgKidney
Porcine800 μg/kgMuscle
300 μg/kgSkin and fat in natural proportions
4 000 μg/kgLiver
8 000 μg/kgKidney