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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)

CELEX
Implementing Regulation (EU) 2015/1492
Date of document
Articles
3
Source
EUR-Lex
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 3 November 2015.

Schedules & Appendices

ANNEX

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

3 articles

Cite this act

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) (EUR-Lex). Retrieved via LawPlayer, https://lawplayer.com/eu/act/32015R1492

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

EU-EurLex-Reuse-2011-833

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