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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 07/25/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) 540/2011
   
Date of approval 01/10/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
EE

DE
Risk Assessment EFSA
Category HB Review Report
Remarks The original RMS was Germany.
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
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Metribuzin
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.013 Dir 07/25  
ARfD 0.02 Dir 07/25  
AOEL 0.02 Dir 07/25  
Other
0.02 AUS 1982 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level