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Commission Implementing Regulation (EU) No 122/2012 ANNEX

Commission Implementing Regulation (EU) No 122/2012 ANNEX

ANNEXSupplementary provisions

ANNEX The entry for methylprednisolone 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 ‘Methylprednisolone Methylprednisolone Bovine 10  μg/kg Muscle   Corticoides/Glucocorticoides’ 10  μg/kg Fat 10  μg/kg Liver 10  μg/kg Kidney 2  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 122/2012 (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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