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MabThera 100 mg/10 ml, Konzentrat zur Herstellung einer Infusionslösung - Professional business directory
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MabThera 100 mg/10 ml, Konzentrat zur Herstellung einer Infusionslösung

Business Listing - September 21, 2024

MabThera 100 mg/10 ml, Konzentrat zur Herstellung einer Infusionslösung

Zulassungs- nummer  / N° d'autorisation : 54378 Dosisstärke-nummer  / N° de dosage : 01 Bezeichnung des Arzneimittels / Dénomination du médicament : MabThera 100 mg/10 ml, Konzentrat zur Herstellung einer Infusionslösung Zulassungsinhaberin / Titulaire de l'autorisation : Roche Pharma (Schweiz) AG Zulassungsart / Type d'autorisation : Hauptzulassung Heilmittelcode / Catégorie du médicament : Biotechnologika Verfahren nach Art. 14 Abs. 1 Bst. abis-quater HMG / Procédures selon l'art.14, al.1, let.abis-quater LPTh : IT-Nummer / No IT : 07.16.1. ATC-Code / Code ATC : L01FA01 Erstzulassungs-datum Arzneimittel / Date de première autorisation du médicament : 27/11/1997 Zul.datum Dosisstärke / Date d'autorisation du dosage : 27/11/1997 Gültigkeitsdauer der Zulassung * / Durée de validité de l'AMM * : unbegrenzt Abgabekategorie Dosisstärke  / Cat. de remise du dosage : A Abgabekategorie Arzneimittel / Cat. de remise du médicament : A Wirkstoff(e) / Principe(s) actif(s) : rituximabum Zusammensetzung / Composition : rituximabum 100 mg, natrii citras dihydricus, polysorbatum 80, natrii chloridum, acidum hydrochloridum aut natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 10 ml corresp. natrium 52.6 mg. Volldeklaration rev. AMZV umgesetzt / Déclaration complète OEMéd rév. implémentée : X Anwendungsgebiet Arzneimittel / Champ d'application du médicament : Non-Hodgkin-Lymphom, Rheumatoide Arthritis, ANCA-assoziierte Vasculitis Anwendungsgebiet Dosisstärke / Champ d'application du dosage : Gentechnisch hergestellte Wirkstoffe / Principes actifs produits par génie génétique : X Kategorie bei Insulinen / Catégorie en cas d'insuline : Verz. bei betäubungsmittelhaltigen Arzneimitteln ** / N° du tabl. Si médicaments à base de stupéfiants ** : Besondere Angaben / Indications particulières : Zulassungsstatus / Statut d'autorisation : zugelassen Befristet zugelassene Indikation(en) / Ablauf Datum / Indication(s) autorisée(s) pour une durée limitée / date d’expiration :
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dosage autorisation medicament arzneimittel dosisstärke nummer datum konzentrat natrii mabthera

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