With no aRM-63/2015-1499 of March 5, 2015 's revoked, pursuant to art. 38, paragraph 9, of the Legislative Decree of April 24, 2006, no. 219, on renunciation of Bausch & Lomb-Iom S.p.a. the marketing authorisation for the medicinal product in the boxes indicated below: Medicine: ARUTIDOR;
Package: 041569031;
Description: "20 mg/ml + 5 mg/ml eye drops" 6 dropper bottles in LDPE from 5 ml;
Medicine: ARUTIDOR;
Package: 041569029;
Description: "20 MG/ml + 5 mg/ml eye drops" 3 dropper bottles in LDPE from 5 ml;
Medicine: ARUTIDOR;
Package: 041569017;
Description: "20 mg/ml + 5 mg/ml eye drops" 1 5 ml dropper bottle from LDPE.
If the distribution channel were present stocks of medicine revoked, in the course of validity, the same will be disposed of not later than 180 days after the date of publication of this determination.