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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2006/74/EC ,
Reg. (EU) 2015/307 ,
Reg. (EU) No 2018/524 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 878/2014
Date of approval 01/06/2007 Expiration of approval 30/04/2019
RMS

Co-RMS
PL

HU
Risk Assessment EFSA
Category HB Review Report   Conditions of approval 2015
  Inclusion 2006
Remarks Extention of approval (Reg (EU) 2018/524)
The original RMS was Ireland.
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, EL, ES, FR, IE, IT, LU, NL, PL, PT, SK, UK HU
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Triclopyr
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.03 Dir 06/74  
ARfD 0.3 Dir 06/74  
AOEL 0.05 Dir 06/74  
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