Commission Regulation (EU) No 890/2010 of 8 October 2010 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 derquantel Text with EEA relevance

• CELEX: Regulation (EU) No 890/2010
• 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 third day following its publication in the Official Journal of the European Union .

It shall apply from 9 April 2012.

Schedules & Appendices

ANNEX

ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the following substance is inserted in alphabetical order:

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

‘Derquantel

Derquantel

Ovine

2  μg/kg

Muscle

Not for use in animals from which milk is produced for human consumption.

Antiparasitic agents/Agents against endoparasites’

40  μg/kg

Fat

20  μg/kg

Liver

5  μg/kg

Kidney