Review Product Marketing Authorisation For Human Use «Cardicor».

Original Language Title: Modifica dell'autorizzazione all'immissione in commercio delmedicinale per uso umano «Cardicor».

Read the untranslated law here:

Retrieved December 16, 2014 V&A/2624 determines the permission of variation: c. 1. z) for the medicine: CARDICOR European procedure: IF 0185/001-006/H//II/044 Mah: RECORDATI pharmaceutical and chemical industries S.P.A., is hereby amended as follows: introduction of Environmental Risk Assessment and Risk Management Plan in relation to authorisations authorised pack sizes in Italy following the mutual recognition procedure.
Inventory disposal lots already products can be kept on the market until the expiration date printed on the label of the medicinal product in accordance with art. 1 paragraph 5 of the AIFA 14/04/2014 # 371 of Determines published in the Official Gazette No. 101 of 03/05/2014.
Date of determination: from the day following that of its publication, to decompress, in Gazzetta Ufficiale della Repubblica Italiana.