Article 1
Open ↗The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Source
Commission Implementing Regulation (EU) 2015/1492 of 3 September 2015 amending Regulation (EU) No 37/2010 as regards the substance ‘tylvalosin’ (Text with EEA relevance)
Commission Implementing Regulation (EU) 2015/1492 of 3 September 2015 amending Regulation (EU) No 37/2010 as regards the substance ‘tylvalosin’ (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
Open ↗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 November 2015.
Supplementary provisions
ANNEXSupplementary provisions
Open ↗ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance 'tylvalosin' 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 ‘Tylvalosin Tylvalosin Porcine 50 μg/kg 50 μg/kg 50 μg/kg 50 μg/kg Muscle Skin and fat Liver Kidney NO ENTRY Anti-infectious agents/Antibiotics’ Poultry 200 μg/kg Eggs Sum of Tylvalosin and 3-0-acetyltylosin Poultry 50 μg/kg 50 μg/kg Skin and fat Liver
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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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