Revoke Authorisation Upon Renunciation, Commerciodel Medicinal Product For Human Use "metformin Sandoz Gmbh».

Original Language Title: Revoca, su rinuncia, dell'autorizzazione all'immissione in commerciodel medicinale per uso umano «Metformina Sandoz GMBH».

Read the untranslated law here: http://www.gazzettaufficiale.it/atto/serie_generale/caricaArticoloDefault/originario?atto.dataPubblicazioneGazzetta=2015-03-18&atto.codiceRedazionale=15A01882&elenco30giorni=false&atto.tipoProvvedimento=DECRETO

With no aRM-40/2015-1771 of February 17, 2015 's revoked, pursuant to art. 38, paragraph 9, of the Legislative Decree of April 24, 2006, no. 219, on renunciation of Sandoz Gmbh the marketing authorisation for the medicinal product in the boxes indicated below.
Medication: METFORMIN SANDOZ GMBH.
Packaging: 038898641-850 mg film-coated tablets» 500 tablets in HDPE;
038898639-«850 mg film-coated tablets» 250 tablets in HDPE;
038898627-«850 mg film-coated tablets» 200 tablets in HDPE;
038898615-«850 mg film-coated tablets» 100 tablets in HDPE;
038898603-«850 mg film-coated tablets» 60 tablets in HDPE;
038898591-«850 mg film-coated tablets» 30 tablets in HDPE;
038898449-«850 mg film-coated tablets» 300 tablets in PVC/AL;
038898437-«850 mg film-coated tablets» 250 tablets in PVC/AL;
038898425-«850 mg film-coated tablets» 180 tablets in PVC/AL;
038898413-«850 mg film-coated tablets» 120 tablets in PVC/AL;
038898401-«850 mg film-coated tablets» 100 tablets in PVC/AL;
038898399-«850 mg film-coated tablets» 90 tablets in PVC/AL;
038898387-«850 mg film-coated tablets» 84 tablets in PVC/AL;
038898375-«850 mg film-coated tablets» 60 tablets in PVC/AL;
038898351-«850 mg film-coated tablets» 50 tablets in PVC/AL;
038898348-«850 mg film-coated tablets» 40 tablets in PVC/AL;
038898336-«850 mg film-coated tablets» 30 tablets in PVC/AL;
038898363-«850 mg film-coated tablets» 56 tablets in PVC/AL;
038898312-«850 mg film-coated tablets» 20 tablets in PVC/AL;
038898300-' 500 mg film-coated tablets» 500 tablets in HDPE;
038898298-' 500 mg film-coated tablets» 400 tablets in HDPE;
038898324-«850 mg film-coated tablets» 28 tablets in PVC/AL;
038898286-' 500 mg film-coated tablets» 250 tablets in HDPE;
038898274-' 500 mg film-coated tablets» 100 tablets in HDPE;
038898262-' 500 mg film-coated tablets» 60 tablets in bottle PE;
038898250-' 500 mg film-coated tablets» 30 tablets in HDPE;
038898122-' 500 mg film-coated tablets» 270 tablets in PVC/AL;
038898110-' 500 mg film-coated tablets» 250 tablets in PVC/AL;
038898108-' 500 mg film-coated tablets» 180 tablets in PVC/AL;
038898096-' 500 mg film-coated tablets» 120 tablets in PVC/ALU: 038898084-«500 mg film-coated tablets» 100 tablets in PVC/AL;
038898072-' 500 mg film-coated tablets» 90 tablets in PVC/AL;
038898060-' 500 mg film-coated tablets» 84 tablets in PVC/AL;
038898058-' 500 mg film-coated tablets» 60 tablets in PVC/AL;
038898045-' 500 mg film-coated tablets» 56 tablets in PVC/AL;
038898033-' 500 mg film-coated tablets» 50 tablets in PVC/AL;
038898021-' 500 mg film-coated tablets» 30 tablets in PVC/AL;
038898019-' 500 mg film-coated tablets» 28 tablets in PVC/AL.
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.