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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 07/5/EC ,
Reg. (EU) 540/2011 ,
Reg. (EU) 2018/917
   
Date of approval 01/10/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
ES

EL
Risk Assessment EFSA
Category IN, AC Review Report
Remarks The original RMS was Italy.
Authorisation at national level
Authorised in In progress for
BE, CY, EL, ES, IT, NL, PL, PT, RO
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Formetanate: Sum of formetanate and its salts expressed as formetanate(hydrochloride)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 2 - H300 Skin Sens. 1 - H317
Acute Tox. 2 - H330 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.004 Dir 07/5  
ARfD 0.005 Dir 07/5  
AOEL 0.004 Dir 07/5  
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