Annex

United Kingdom

The entry corresponding to diclazuril in Table 1 of the Annex to Regulation (EU) No 37/2010 is replaced by the following:

Pharmacologically active Substance Marker residue Animal Species MRL Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic Classification
‘Diclazuril NOT APPLICABLE All ruminants, porcine No MRL required NOT APPLICABLE For oral use only NO ENTRY
Poultry 500 μg/kg Muscle Not for use in animals from which eggs are produced for human consumption Antiparasitic agents/Agents acting againsts protozoa’
500 μg/kg Skin and fat in natural proportions
1 500 μg/kg Liver
1 000 μg/kg Kidney

Pharmacologically active Substance	Marker residue	Animal Species	MRL	Target Tissues	Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009)	Therapeutic Classification
‘Diclazuril	NOT APPLICABLE	All ruminants, porcine	No MRL required	NOT APPLICABLE	For oral use only	NO ENTRY
		Poultry	500 μg/kg	Muscle	Not for use in animals from which eggs are produced for human consumption	Antiparasitic agents/Agents acting againsts protozoa’
			500 μg/kg	Skin and fat in natural proportions
			1 500 μg/kg	Liver
			1 000 μg/kg	Kidney