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Napropamide Approved
Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
| Legislation |
2010/83/EU
, Reg. (EU) 2018/670 , Reg. (EU) No 540/2011 |
||
|---|---|---|---|
| Date of approval | 01/01/2011 | Expiration of approval | 31/12/2023 |
| RMS
Co-RMS |
SI
HR |
Risk Assessment | EFSA |
| Category | HB | Review Report |
Review report 2017
Inclusion 2010 |
| Remarks | Initially non included by Decision 2008/902. Inclusion voted in SCoFCAH Oct 2010 following re-submission for inclusion according to Reg. 33/2008 | ||
Authorisation at national level
| Authorised in | In progress for |
|---|---|
| AT, BE, BG, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, RO, SE, SI, SK, UK |
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
| Legislation | Annexes |
|---|---|
|
Classification Reg. 1272/2008
| No classification |
Toxicological information
| Reference values | Source | Remark | |
|---|---|---|---|
| ADI | 0.3 | 10/83/EU | |
| ARfD | Not applicable | 10/83/EU | |
| AOEL | 0.5 | 10/83/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