Glipizid fice

Hauptinformation

  • Handelsname:
  • Glipizid fice Tablette
  • Darreichungsform:
  • Tablette
  • Zusammensetzung:
  • Glipizid 5.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:
  • Glipizid fice Tablette
    Deutschland
  • Sprache:
  • Deutsch

Weitere Informationen

Status

  • Quelle:
  • BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte
  • Zulassungsnummer:
  • 29894.00.00
  • Letzte Änderung:
  • 01-12-2018

18-12-2018


eXtended EudraVigilance Medicinal Product Dictionary face-to-face training course (Basel), DIA EMEA Office, Basel Switzerland, from 27/06/2019 to 28/06/2019

eXtended EudraVigilance Medicinal Product Dictionary face-to-face training course (Basel), DIA EMEA Office, Basel Switzerland, from 27/06/2019 to 28/06/2019

eXtended EudraVigilance Medicinal Product Dictionary face-to-face training course (Basel), DIA EMEA Office, Basel Switzerland, from 27/06/2019 to 28/06/2019

Europe - EMA - European Medicines Agency

28-9-2018

Debate on research dissemination at the Danish Medicines Agency

Debate on research dissemination at the Danish Medicines Agency

On 1 October, the Danish Medicines Agency and the Danish Society for Pharmacoepidemiology have invited a number of researchers, doctors and communication officers from research institutions throughout Denmark to a debate on how the findings of new health research can be disseminated most responsibly. The debate meeting can be followed live on the Danish Medicines Agency’s Facebook profile.

Danish Medicines Agency

10-9-2018

"My Medicines" ... This Brochure Can be a Lifesaver

"My Medicines" ... This Brochure Can be a Lifesaver

"My Medicines" a brochure offered by FDA's Office of Women's Health, can play a vital role in the medical treatment you receive during an emergency.

FDA - U.S. Food and Drug Administration

18-6-2018

June 15, 2018: Theranos Founder and Former Chief Operating Officer Charged in Alleged Wire Fraud Schemes

June 15, 2018: Theranos Founder and Former Chief Operating Officer Charged in Alleged Wire Fraud Schemes

June 15, 2018: Theranos Founder and Former Chief Operating Officer Charged in Alleged Wire Fraud Schemes

FDA - U.S. Food and Drug Administration

4-6-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on proposed modernization of FDA’s drug review office

Statement from FDA Commissioner Scott Gottlieb, M.D., on proposed modernization of FDA’s drug review office

FDA has proposed an important series of new steps to modernize the organization and functions of CDER’s Office of New Drugs.

FDA - U.S. Food and Drug Administration

22-5-2018

May 21, 2018: Oncologist and Office Manager Sentenced in Connection with Administering Unapproved, Foreign Drugs

May 21, 2018: Oncologist and Office Manager Sentenced in Connection with Administering Unapproved, Foreign Drugs

May 21, 2018: Oncologist and Office Manager Sentenced in Connection with Administering Unapproved, Foreign Drugs

FDA - U.S. Food and Drug Administration

9-5-2018

Medication Safety: Advice for New Parents

Medication Safety: Advice for New Parents

Mother's Day and Father's Day are exciting for new parents. But moms and dads of babies 12 months and younger can also have some worries. Medical officers at the U.S. Food and Drug Administration offer health suggestions.

FDA - U.S. Food and Drug Administration

25-5-2018

Therapeutic Goods (Medicines-Listing) Approval of Application Forms and Specification of Office to which Application Must be Delivered

Therapeutic Goods (Medicines-Listing) Approval of Application Forms and Specification of Office to which Application Must be Delivered

I, Larry Kelly, Acting Deputy Secretary, Health Products Regulation Group, a delegate of the Secretary of the Department of Health for the purposes of section 23C of the Therapeutic Goods Act 1989, make the following instrument under paragraphs 23C(2)(a...

Therapeutic Goods Administration - Australia

24-5-2018

#ThrowBackThursday- May 24, 1977- Bureau of Medical Devices and Diagnostic Products renamed Bureau of Medical Devices and new Office of Small Manufacturers Assistance created, as required by law. #OnThisDay #FDAHistory

#ThrowBackThursday- May 24, 1977- Bureau of Medical Devices and Diagnostic Products renamed Bureau of Medical Devices and new Office of Small Manufacturers Assistance created, as required by law. #OnThisDay #FDAHistory

#ThrowBackThursday- May 24, 1977- Bureau of Medical Devices and Diagnostic Products renamed Bureau of Medical Devices and new Office of Small Manufacturers Assistance created, as required by law. #OnThisDay #FDAHistory

FDA - U.S. Food and Drug Administration