Commission Implementing Regulation (EU) No 201/2012 ANNEX

ANNEXSupplementary provisions

ANNEX The entry corresponding to nitroxinil 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 ‘Nitroxinil Nitroxinil Bovine, ovine 400 μg/kg Muscle Antiparasitic agents/agents against endoparasites’ 200 μg/kg Fat 20 μg/kg Liver 400 μg/kg Kidney 20 μg/kg Milk

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Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationANNEX of Commission Implementing Regulation (EU) No 201/2012 (LawPlayer, data as of 2026-07-04)

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