PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
    Old Legislation 07/25/EC ,
Reg. (EU) No 2015/404 ,
Reg. (EU) No 2015/845 ,
Reg. (EU) No 365/2013 ,
Reg. (EU) No 540/2011
RMS

Co-RMS
DE

FR
Risk Assessment EFSA
Category HB Review Report   Inclusion 2007
  Conditions of approval 2013
Remarks The original RMS was Sweden.

Toxic for reproduction 1A / 1B

Authorisation at national level
Authorised in In progress for
BE, BG, CZ, EL, HR, HU, PL, PT, RO, SK, UK CY
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Glufosinate-ammonium (sum of glufosinate, its salts, MPP and NAG expressed as glufosinate equivalents)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Acute Tox. 4 - H312
Acute Tox. 4 - H332 Repr. 1B - H360FD
STOT RE 2 - H373  
Toxicological information
Reference values Source Remark
ADI 0.021 Dir 07/25  
ARfD 0.021 Dir 07/25  
AOEL 0.0021 Dir 07/25  
Other
ARfD unnecessary ADI 0,02 JMPR 1999 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level