Provigil 100 mg Tabletten

Hauptinformation

  • Handelsname:
  • Provigil 100 mg Tabletten
  • Darreichungsform:
  • Tablette
  • Zusammensetzung:
  • Modafinil 100.mg
  • 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:
  • Provigil 100 mg Tabletten
    Deutschland
  • Sprache:
  • Deutsch

Weitere Informationen

Status

  • Quelle:
  • BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte
  • Zulassungsnummer:
  • 94742.00.00
  • Letzte Änderung:
  • 14-12-2018

4-12-2018

Arnica compositum ad us. vet., Tabletten

Arnica compositum ad us. vet., Tabletten

● Die Neuzulassung erfolgte am 04.12.2018.

Institut für Veterinärpharmakologie und toxikologie

23-11-2018

UpCard ad us. vet. 0,75 mg, teilbare Tabletten

UpCard ad us. vet. 0,75 mg, teilbare Tabletten

● Die Neuzulassung erfolgte am 23.11.2018.

Institut für Veterinärpharmakologie und toxikologie

23-11-2018

UpCard ad us. vet. 3 mg, teilbare Tabletten

UpCard ad us. vet. 3 mg, teilbare Tabletten

● Die Neuzulassung erfolgte am 23.11.2018.

Institut für Veterinärpharmakologie und toxikologie

23-11-2018

UpCard ad us. vet. 7,5 mg, teilbare Tabletten

UpCard ad us. vet. 7,5 mg, teilbare Tabletten

● Die Neuzulassung erfolgte am 23.11.2018.

Institut für Veterinärpharmakologie und toxikologie

22-11-2018

Foreign Product Alert: Black Lion Pill, Help 100% & Pure Natural & Body Slim capsules, Herba Saraf, Horny Little Devil, Ja Dera Max capsules, Lida (Plus) capsules, Nutra Organics Green Tea Extract capsules, Papapa, Red Zone Xtreme 3000, Rhino 69 Extreme 5

Foreign Product Alert: Black Lion Pill, Help 100% & Pure Natural & Body Slim capsules, Herba Saraf, Horny Little Devil, Ja Dera Max capsules, Lida (Plus) capsules, Nutra Organics Green Tea Extract capsules, Papapa, Red Zone Xtreme 3000, Rhino 69 Extreme 5

These foreign health products have been found by regulators in other countries to contain undeclared drug ingredients and/or unacceptable contaminant(s).

Health Canada

22-11-2018

Safety and efficacy of Monteban® G100 (narasin) for ducks for fattening

Safety and efficacy of Monteban® G100 (narasin) for ducks for fattening

Published on: Wed, 21 Nov 2018 Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of Monteban® G100 for ducks. Monteban® G100, containing narasin, is intended for the prevention of coccidiosis in ducks for fattening at a dose range of 60–70 mg/kg of complete feed. Narasin from Monteban® G100 is safe for ducks for fattening at a level of 70 mg/kg complete feed...

Europe - EFSA - European Food Safety Authority Publications

21-11-2018

VaperBC recalls 100 mg Nicotine Base Liquid Nicotine

VaperBC recalls 100 mg Nicotine Base Liquid Nicotine

These vaping products do not meet requirements of the Consumer Chemicals and Containers Regulations, 2001 (CCCR, 2001) under the Canada Consumer Product Safety Act.

Health Canada

21-11-2018

Safety and efficacy of Monteban® G100 (narasin) for chickens for fattening

Safety and efficacy of Monteban® G100 (narasin) for chickens for fattening

Published on: Tue, 20 Nov 2018 The feed additive Monteban® G100, containing the active substance narasin, an ionophore anticoccidial, is intended to control coccidiosis in chickens for fattening at a dose of 60–70 mg/kg complete feed. Narasin is produced by fermentation. Limited data on the taxonomic identification of the production strain did not allow the proper identification of strain NRRL 8092 as Streptomyces aureofaciens. The FEEDAP Panel cannot conclude on the absence of genetic determinants for ...

Europe - EFSA - European Food Safety Authority Publications

12-12-2018

Therapeutic Goods (Microbiological Standards for Medicines) (TGO 100) Order 2018

Therapeutic Goods (Microbiological Standards for Medicines) (TGO 100) Order 2018

TGO 100 has been registered on the Federal Register of Legislation. It commences on 8 December 2018, repealing and replacing TGO 98

Therapeutic Goods Administration - Australia

11-12-2018

Concor 5 mg/10 mg Filmtabletten

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11-12-2018

Ubretid® Tabletten 5,0 mg

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11-12-2018

Biofanal 100 000 I.E. Salbe

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11-12-2018

Quetiapin TAD® 400 mg Retardtabletten

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7-12-2018

EZETROL 10 mg Tabletten

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7-12-2018

Lendormin® 0,25 mg Tabletten

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7-12-2018

Diabact UBT 50 mg Tabletten

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6-12-2018

Imanivec® 400 mg Filmtabletten

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6-12-2018

ABILIFY® Tabletten

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6-12-2018

ABILIFY® Schmelztabletten

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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

Cliovelle® 1 mg/0,5 mg Tabletten

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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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1-12-2018

SEMPERA® Kapseln, 100 mg Hartkapseln

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1-12-2018

SIROS® Kapseln, 100 mg Hartkapseln

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29-11-2018

Arpilif 5 mg / -15 mg Tabletten

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29-11-2018

Arpilif 10 mg / -30 mg Tabletten

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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

Ramipril comp. AbZ Tabletten

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27-11-2018

Olmedipin Filmtabletten

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27-11-2018

Paroxetin-ratiopharm 40 mg Tabletten

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27-11-2018

Nevirapin-ratiopharm® 200 mg Tabletten

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23-11-2018

Combivir Filmtabletten

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22-11-2018

Damara® 75 Mikrogramm Filmtabletten

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21-11-2018

EU/3/18/2100 (Quality Regulatory Clinical Ireland Limited)

EU/3/18/2100 (Quality Regulatory Clinical Ireland Limited)

EU/3/18/2100 (Active substance: Propagermanium) - Orphan designation - Commission Decision (2018)7810 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/103/18

Europe -DG Health and Food Safety