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Commission Implementing Regulation (EU) 2015/149 ANNEX

Commission Implementing Regulation (EU) 2015/149 ANNEX

ANNEXSupplementary provisions

ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘methylprednisolone’ is replaced by the following: Pharmacologically active Substance Marker residue Animal Species MRLs Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic Classification ‘Methylprednisolone Methylprednisolone Equidae 10 μg/kg 10 μg/kg 10 μg/kg 10 μg/kg 2 μg/kg Muscle Fat Liver Kidney Milk NO ENTRY Corticoides/Glucocorticoides’ Bovine 10 μg/kg 10 μg/kg 10 μg/kg 10 μg/kg 2 μg/kg Muscle Fat Liver Kidney Milk NO ENTRY

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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) 2015/149 (LawPlayer, data as of 2026-07-04)

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

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