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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2017/2091 Old Legislation 03/31/EC ,
Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1511 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
    Expiration of approval 05/03/2018
RMS

Co-RMS
FR

BE
Risk Assessment EFSA
Category FU, NE Review Report   New Reference Values (2018).pdf
  Non renewal Review report 2017
  Review report 2002
Remarks Withdrawal authoris. by 5/03/2018. Max period of grace: 5/06/2018.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EL, ES, FI, IT, LT, LU, LV, MT, NL, PL, PT, SI, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Iprodione (R)
    MRLs Annex II
Classification Reg. 1272/2008
Carc. 2 - H351 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.02 Reg. (EU) 2017/2091  
ARfD 0.06 Reg. (EU) 2017/2091  
AOEL 0.04 Reg. (EU) 2017/2091  
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