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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/34/EC ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 58/2015
   
Date of approval 01/06/2005 Expiration of approval 31/05/2015
RMS ES

Risk Assessment Commission
Category HB Review Report
Authorisation at national level
Authorised in In progress for
NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Tepraloxydim (sum of tepraloxydim and its metabolites that can be hydrolysed either to the moiety 3-(tetrahydro-pyran-4-yl)-glutaric acid or to the moiety 3-hydroxy-(tetrahydro-pyran-4-yl)-glutaric acid, expressed as tepraloxydim)
    MRLs Annex II
Classification Reg. 1272/2008
Carc. 2 - H351 Repr. 2 - H361fd
Toxicological information
Reference values Source Remark
ADI 0.025 05/34/EC  
ARfD 0.4 05/34/EC  
AOEL 0.06 05/34/EC  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level