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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 820/2011 Old Legislation 2008/934/EC
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
ES

HR
Risk Assessment EFSA
Category HB Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EL, ES, FR, HR, HU, IE, IT, LU, MT, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Terbuthylazine
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.004 Reg. (EU) No 820/2011  
ARfD 0.008 Reg. (EU) No 820/2011  
AOEL 0.0032 Reg. (EU) No 820/2011  
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