Article 1
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
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
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
Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
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 .
Supplementary provisions
ANNEXSupplementary provisions
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’
Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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