Commission Implementing Regulation (EU) No 394/2013 of 29 April 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 monepantel Text with EEA relevance

• CELEX: Implementing Regulation (EU) No 394/2013
• 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 29 June 2013.

Schedules & Appendices

ANNEX

ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry corresponding to monepantel 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

‘Monepantel

Monepantel-sulfone

Ovine, caprine

700  μg/kg

Muscle

Antiparasitic agents/Agents acting against endoparasites’

7 000  μg/kg

Fat

5 000  μg/kg

Liver

2 000  μg/kg

Kidney

170  μg/kg

Milk