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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 595/2012 Old Legislation Dossier complete 2010/150/EU
Date of approval 01/01/2013 Expiration of approval 31/12/2022
RMS

Co-RMS
LV

LT
Risk Assessment EFSA
Category FU Review Report
Remarks The original RMS was Austria.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EL, ES, FI, FR, 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
  • Fenpyrazamine
    MRLs Annex II
Classification Reg. 1272/2008
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.13 Reg. (EU) No 595/2012  
ARfD 0.3 Reg. (EU) No 595/2012  
AOEL 0.2 Reg. (EU) No 595/2012  
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