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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/83/EU ,
Reg. (EU) 2018/670 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2011 Expiration of approval 31/12/2023
RMS

Co-RMS
SI

HR
Risk Assessment EFSA
Category HB Review Report   Review report 2017
  Inclusion 2010
Remarks Initially non included by Decision 2008/902. Inclusion voted in SCoFCAH Oct 2010 following re-submission for inclusion according to Reg. 33/2008
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Napropamide
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.3 10/83/EU  
ARfD Not applicable 10/83/EU  
AOEL 0.5 10/83/EU  
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