Commission Implementing Regulation (EU) 2025/1105 of 3 June 2025 amending Regulation (EU) No 37/2010 as regards the classification of the substance ketoprofen with respect to its maximum residue limit in foodstuffs of animal origin

• CELEX: Implementing Regulation (EU) 2025/1105
• 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 .

Schedules & Appendices

ANNEX

ANNEX

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

‘Ketoprofen

Ketoprofen

All ruminants,

porcine,

Equidae

50 μg/kg

20 μg/kg

20 μg/kg

50 μg/kg

20 μg/kg

Muscle

Fat

Liver

Kidney

Milk

For porcine species the fat MRL relates to ‘skin and fat in natural proportions’

NO ENTRY

Ketoprofen

Poultry

10 μg/kg

30 μg/kg

10 μg/kg

10 μg/kg

Muscle

Skin and fat in natural proportion

Liver

Kidney

Not for use in animals from which eggs are produced for human consumption

NO ENTRY’