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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
    Old Legislation 07/25/EC ,
Reg. (EU) 2015/845 ,
Reg. (EU) No 365/2013 ,
Reg. (EU) No 540/2011
Date of approval 01/10/2007 Expiration of approval 31/07/2018
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
AT, BE, BG, CZ, EE, EL, FR, HR, HU, IE, IT, LU, LV, NL, PL, PT, RO, SI, 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