Commission Implementing Regulation (EU) No 406/2013 of 2 May 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 prednisolone Text with EEA relevance

• CELEX: Implementing Regulation (EU) No 406/2013
• 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 3 July 2013.

Schedules & Appendices

ANNEX

ANNEX

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

‘Prednisolone

Prednisolone

Bovine

4  μg/kg

Muscle

NO ENTRY

Corticoids/Glucocorticoids’

4  μg/kg

Fat

10  μg/kg

Liver

10  μg/kg

Kidney

6  μg/kg

Milk

Equidae

4  μg/kg

Muscle

8  μg/kg

Fat

6  μg/kg

Liver

15  μg/kg

Kidney