Review Product Marketing Authorisation For Human Use "imipenem And Cilastatin Kabi».

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

Read the untranslated law here:

Retrieved December 16, 2014 V&A/2628 of authorization determines variation: B z relative to medicine: IMIPENEM and CILASTATIN KABI European procedure: UK/H/1334/002/II/014 Mah: FRESENIUS KABI ITALIA S.R.L., is hereby amended as of setuito States: update of the DMF (ACS Dobfar) from version 1 "[1.9.2009] and 2 [01/2011] [06/2013] version 3" and "4 [10/2013]" for the active ingredient of Imipenem sterile.
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 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.