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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/66 ,
Reg. (EU) No 2018/1796 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2019
RMS

Co-RMS
CZ

DE
Risk Assessment EFSA
Category FU Review Report   Inclusion 2008
  Confirmatory data 2012
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fenpropidin (sum of fenpropidin and its salts, expressed as fenpropidin) (R) (A)
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.02 Dir 08/66  
ARfD 0.02 Dir 08/66  
AOEL 0.02 Dir 08/66  
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