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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 02/64/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
Old Legislation 2010/77/EU ,
Reg. (EU) 2015/1885 ,
Reg. (EU) 2016/549 ,
Reg. (EU) 2017/841
Date of approval 01/10/2002 Expiration of approval 30/06/2019
RMS

Co-RMS
UK

FI
Risk Assessment Commission
Category FU Review Report
Remarks FR was RMS for the inclusion.
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EL, ES, FR, HR, HU, IT, MT, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Famoxadone (F)
    MRLs Annex II
Classification Reg. 1272/2008
STOT RE 2 - H373 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.012 02/64/EC  
ARfD 0.2 02/64/EC  
AOEL 0.0048 02/64/EC  
Other
ARfD 0,6 - ADI 0,006 JMPR 2003 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level