Commission Implementing Regulation (EU) 2016/1444 of 31 August 2016 amending Regulation (EU) No 37/2010 as regards the substance hydrocortisone aceponate (Text with EEA relevance)

• CELEX: Implementing Regulation (EU) 2016/1444
• 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 31 October 2016.

Schedules & Appendices

ANNEX

ANNEX

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

‘Hydrocortisone aceponate

Sum of hydrocortisone and its esters after alkaline hydrolysis expressed as hydrocortisone

All ruminants, Equidae

10 μg/kg

Milk

For intramammary use only

Corticosteroids’

NOT APPLICABLE

All ruminants, Equidae

No MRL required for all tissues except milk

NOT APPLICABLE