OLD BROWSER ! We have noticed that you are using an old Internet browser. For a better browsing experience, we recommend that you use a different browser or upgrade to a newer version of your browser.
Reg. (EU) No 2018/1266 ,
Reg. (EU) No 540/2011
|Date of approval||01/06/2011||Expiration of approval||31/05/2023|
Confirmatory data 2014
Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008.
The original RMS was UK.
|Type||Candidate for Substitution (CfS)||CfS - criteria||two PBT criteria|
Authorisation at national level
|Authorised in||In progress for|
|AT, BE, BG, CZ, DE, DK, EE, ES, FI, FR, HU, IE, IT, LT, LV, NL, RO, SE, SK, UK||EL|
Classification Reg. 1272/2008
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level