Commission Implementing Regulation (EU) No 1390/2014 of 19 December 2014 amending the Annex to Regulation (EU) No 37/2010, as regards the substance ‘eprinomectin’ Text with EEA relevance

• CELEX: Implementing Regulation (EU) No 1390/2014
• 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 22 February 2015.

Schedules & Appendices

ANNEX

ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘eprinomectin’ 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

‘Eprinomectin

Eprinomectin B1a

Bovine

50 μg/kg

250 μg/kg

1 500 μg/kg

300 μg/kg

20 μg/kg

Muscle

Fat

Liver

Kidney

Milk

NO ENTRY

Antiparasitic agents/Agents acting against endo- and ectoparasites’

Ovine, caprine

50 μg/kg

250 μg/kg

1 500 μg/kg

300 μg/kg

20 μg/kg

Muscle

Fat

Liver

Kidney

Milk

Provisional maximum residue limits expire on 30 June 2016