Commission Implementing Regulation (EU) No 201/2012 of 8 March 2012 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 nitroxinil Text with EEA relevance

• CELEX: Implementing Regulation (EU) No 201/2012
• 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 8 May 2012.

Schedules & Appendices

ANNEX

ANNEX

The entry corresponding to nitroxinil 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

‘Nitroxinil

Nitroxinil

Bovine, ovine

400  μg/kg

Muscle

Antiparasitic agents/agents against endoparasites’

200  μg/kg

Fat

20  μg/kg

Liver

400  μg/kg

Kidney

20  μg/kg

Milk