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Commission Implementing Regulation (EU) No 85/2012 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 altrenogest Text with EEA relevance

Commission Implementing Regulation (EU) No 85/2012 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 altrenogest Text with EEA relevance

Implementing Regulation (EU) No 85/2012 · Regulation · 3 articles

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 1

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The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

Article 2

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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

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ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance altrenogest 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 ‘Altrenogest Altrenogest Porcine 4  μg/kg Skin and fat Only for zootechnical use and in accordance with the provisions of Directive 96/22/EC Agents acting on the reproductive system’ 2  μg/kg Liver Equidae 4  μg/kg Fat 4  μg/kg 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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