Commission Implementing Regulation (EU) No 115/2013 of 8 February 2013 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril Text with EEA relevance

• CELEX: Implementing Regulation (EU) No 115/2013
• Articles: 3

Article 1

The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

Article 2

This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .

It shall apply from 10 April 2013.

Schedules & Appendices

ANNEX

ANNEX

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