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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/37 ,
Reg. (EU) No 540/2011
   
Date of approval 01/12/2009 Expiration of approval 30/11/2021
RMS

Co-RMS
AT

EE
Risk Assessment EFSA
Category HB Review Report
Remarks Extension of the approval period: Reg. (EU) 2017/555

The original RMS was UK.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Propaquizafop
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.015 EFSA 08  
ARfD Not applicable EFSA 08  
AOEL 0.04 EFSA 08  
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