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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/44/EU ,
Reg. (EU) No 2018/1266 ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2024
RMS

Co-RMS
DE

ES
Risk Assessment EFSA
Category IN Review Report
Remarks Initially non included by Decision 2008/941. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, HU, IT, LT, LU, LV, NL, PT, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Azadirachtin
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.1 11/44/EU  
ARfD 0.75 11/44/EU  
AOEL 0.1 11/44/EU  
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