The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
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Commission Implementing Regulation (EU) 2015/149 of 30 January 2015 amending the Annex to Regulation (EU) No 37/2010 as regards the substance ‘methylprednisolone’ Text with EEA relevance
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 1 April 2015.
Schedules & Appendices
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
Cite this act
Commission Implementing Regulation (EU) 2015/149 of 30 January 2015 amending the Annex to Regulation (EU) No 37/2010 as regards the substance ‘methylprednisolone’ Text with EEA relevance (EUR-Lex). Retrieved via LawPlayer, https://lawplayer.com/eu/act/32015R0149
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