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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/15/EU ,
Reg. (EU) 2017/1527 ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2010 Expiration of approval 31/05/2023
RMS

Co-RMS
AT

ES
Risk Assessment EFSA
Category FU Review Report
Remarks Extension of approval period: Reg. (EU) 2017/1527

The original RMS was UK.
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, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.08 2010/15/EU  
ARfD 0.18 2010/15/EU  
AOEL 0.05 2010/15/EU  
Other
Metabolite 2,6-dichlorobenzamide: ADI= 0.05 ARfD= 0,3 (EFSA ´09) 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level