Octegra 400 mg Filmtabletten

Hauptinformation

  • Handelsname:
  • Octegra 400 mg Filmtabletten
  • Einheiten im Paket:
  • 1 Stück (Aluminium/Aluminiumblister), Laufzeit: 60 Monate,5 Stück (Polyproylen farblos/Aluminiumblister), Laufzeit: 60 Monate,7
  • Verwenden für:
  • Menschen
  • Art der Medizin:
  • allopathic Droge

Dokumenten

  • für die Allgemeinheit:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie das Informationsblatt für die Öffentlichkeit.

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Octegra 400 mg Filmtabletten
    Österreich
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiebereich:
  • Moxifloxacin

Weitere Informationen

Status

  • Quelle:
  • AGES
  • Zulassungsnummer:
  • 1-23495
  • Letzte Änderung:
  • 07-11-2016

1-12-2018

Safety evaluation of the food enzyme endo‐1,4‐β‐xylanase from a genetically modified Trichoderma reesei (strain DP‐Nzd22)

Safety evaluation of the food enzyme endo‐1,4‐β‐xylanase from a genetically modified Trichoderma reesei (strain DP‐Nzd22)

Published on: Fri, 30 Nov 2018 The food enzyme endo‐1,4‐β‐xylanase (EC 3.2.1.8) is produced with a genetically modified Trichoderma reesei (strain DP‐Nzd22) by DuPont. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. The endo‐1,4‐β‐xylanase is intended to be used in distilled alcohol production, bakery and brewery. Residual amounts of total organic solids (TOS) are removed during the production of dis...

Europe - EFSA - European Food Safety Authority Publications

28-11-2018

Prenoxad 1 mg/mL solution for injection (naloxone hydrochloride)

Prenoxad 1 mg/mL solution for injection (naloxone hydrochloride)

Update - medicine shortage

Therapeutic Goods Administration - Australia

13-11-2018

Felimazole 2.5 mg ad us. vet., Filmtabletten fuer Katzen

Felimazole 2.5 mg ad us. vet., Filmtabletten fuer Katzen

● Änderung Text "Anwendungseinschränkungen", "Wechselwirkungen" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

13-11-2018

Felimazole 5 mg ad us. vet., Filmtabletten fuer Katzen

Felimazole 5 mg ad us. vet., Filmtabletten fuer Katzen

● Änderung Text "Anwendungseinschränkungen", "Wechselwirkungen" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

1-11-2018

Safety evaluation of the food enzyme α‐amylase from a genetically modified Aspergillus niger (strain NZYM‐MC)

Safety evaluation of the food enzyme α‐amylase from a genetically modified Aspergillus niger (strain NZYM‐MC)

Published on: Wed, 31 Oct 2018 00:00:00 +0100 The food enzyme alpha‐amylase (4‐α‐d‐glucan glucanohydrolase; EC 3.2.1.1) is produced with the genetically modified strain of Aspergillus niger by Novozymes A/S. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. This α‐amylase is intended to be used in starch processing for glucose syrups production, beverage alcohol (distilling) processes and baking proces...

Europe - EFSA - European Food Safety Authority Publications

14-12-2018

OCALIVA® 5 mg / 10 mg Filmtabletten

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14-12-2018

Nystatin acis® Filmtabletten

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14-12-2018

Seroxat 20 mg Filmtabletten

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13-12-2018

Bisoprolol comp. AbZ Filmtabletten

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13-12-2018

Efavirenz Teva 600 mg Filmtabletten

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13-12-2018

Ursofalk® 500mg Filmtabletten

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13-12-2018

Zolpidem-ratiopharm 5 mg Filmtabletten

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11-12-2018

Concor 5 mg/10 mg Filmtabletten

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11-12-2018

Quetiapin TAD® 400 mg Retardtabletten

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6-12-2018

Imanivec® 400 mg Filmtabletten

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6-12-2018

Tioblis® Filmtabletten

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6-12-2018

Imanivec® 100 mg Filmtabletten

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5-12-2018

Levetiracetam UCB® Filmtabletten

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5-12-2018

Forxiga® 5 mg/10 mg Filmtabletten

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5-12-2018

Uniphyllin® 300 mg/400 mg/600 mg

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4-12-2018

GINKGOVITAL Heumann® Filmtabletten

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4-12-2018

Telzir 700 mg Filmtabletten

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3-12-2018

Alunbrig® Filmtabletten

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1-12-2018

SYLVANT® 100 mg / 400 mg

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28-11-2018

Econor (Elanco GmbH)

Econor (Elanco GmbH)

Econor (Active substance: Valnemulin hydrochloride) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8038 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/42/T/54

Europe -DG Health and Food Safety

28-11-2018

Deferipron Lipomed 500 mg Filmtabletten

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28-11-2018

Xadago 50 mg / 100 mg Filmtabletten

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28-11-2018

Baraclude® 0,5 mg/1 mg Filmtabletten

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27-11-2018

Olmedipin Filmtabletten

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26-11-2018

Wakix (Bioprojet Pharma)

Wakix (Bioprojet Pharma)

Wakix (Active substance: Pitolisant hydrochloride) - Centralised - Yearly update - Commission Decision (2018)7974 of Mon, 26 Nov 2018

Europe -DG Health and Food Safety

23-11-2018

Combivir Filmtabletten

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22-11-2018

Damara® 75 Mikrogramm Filmtabletten

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21-11-2018

EU/3/18/2082 (Takeda Pharma A/S)

EU/3/18/2082 (Takeda Pharma A/S)

EU/3/18/2082 (Active substance: 5-{(1R,2R)-2-[(cyclopropylmethyl)amino]cyclopropyl}-N-(tetrahydro-2H-pyran-4-yl)thiophene-3-carboxamide monohydrochloride) - Orphan designation - Commission Decision (2018)7791 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/040/18

Europe -DG Health and Food Safety

21-11-2018

Epivir 150 / 300 mg Filmtabletten

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20-11-2018

Qlaira® Filmtabletten

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20-11-2018

SUSTIVA® 600 mg Filmtabletten

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16-11-2018

Fycompa® Filmtabletten

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15-11-2018

Sevredol® 10 mg/20 mg Filmtabletten

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14-11-2018

Plavix® Filmtabletten

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14-11-2018

DuoPlavin® 75 mg/100 mg Filmtabletten

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14-11-2018

Iscover® 75 mg Filmtabletten

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13-11-2018

EU/3/17/1836 (Zogenix GmbH)

EU/3/17/1836 (Zogenix GmbH)

EU/3/17/1836 (Active substance: Fenfluramine hydrochloride) - Transfer of orphan designation - Commission Decision (2018)7576 of Tue, 13 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/233/16/T/01

Europe -DG Health and Food Safety

13-11-2018

EU/3/13/1219 (Zogenix GmbH)

EU/3/13/1219 (Zogenix GmbH)

EU/3/13/1219 (Active substance: Fenfluramine hydrochloride) - Transfer of orphan designation - Commission Decision (2018)7575 of Tue, 13 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/140/13/T/01

Europe -DG Health and Food Safety

13-11-2018

Relifex® 500 mg Filmtabletten

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12-11-2018

Actonel® 30 mg Filmtabletten

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12-11-2018

Clopidogrel AbZ 75 mg Filmtabletten

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12-11-2018

Actonel® 5 mg Filmtabletten

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12-11-2018

Actonel® 75 mg Filmtabletten

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8-11-2018

Zydelig® Filmtabletten

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6-11-2018

Symkevi® 100 mg/150 mg Filmtabletten

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2-11-2018

Tramundin® 50 mg Filmtabletten

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1-11-2018

Dexdomitor (Orion Corporation)

Dexdomitor (Orion Corporation)

Dexdomitor (Active substance: dexmedetomidine hydrochloride) - Centralised - Yearly update - Commission Decision (2018)7380 of Thu, 01 Nov 2018

Europe -DG Health and Food Safety