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) No 86/2012 of 1 February 2012 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 lasalocid Text with EEA relevance
Commission Implementing Regulation (EU) No 86/2012 of 1 February 2012 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 lasalocid Text with EEA relevance
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 third day following its publication in the Official Journal of the European Union . It shall apply from 2 April 2012.
Supplementary provisions
ANNEXSupplementary provisions
ANNEX The entry for lasalocid in Table 1 of the Annex to Regulation (EU) No 37/2010 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 ‘Lasalocid Lasalocid A Poultry 20 μg/kg Muscle NO ENTRY Anti-infectious agents/Antibiotics’ 100 μg/kg Skin and fat 100 μg/kg Liver 50 μg/kg Kidney 150 μg/kg Eggs Bovine 10 μg/kg Muscle Not for use in animals from which milk is produced for human consumption 20 μg/kg Fat 100 μg/kg Liver 20 μg/kg Kidney
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