Review Product Marketing Authorisation For Human Use «Panoxyl».

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

Read the untranslated law here:

Retrieved 16 January 14, 2015 V&A determines the Permission for variation/: B z) for the medicine: PANOXYL European procedure: UK/H/192/001/II/022 Mah: Stiefel Laboratories (Ireland) LTD is hereby amended as follows: updating the ASMF manufacturer (Arkema Inc. 3289 Genesee Street, Piffard, NY 14533, USA) (AP/201211; RP/201211) to the active ingredient benzoyl peroxide hydrate with regard to marketing 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 causes of the April 14, 2014 # 371 AIFA published in Official Gazette No 101 of May 3, 2014.
Date of determination: from the day following that of its publication, to decompress, in Gazzetta Ufficiale della Repubblica Italiana.