Pharmacopoeia

Authors: Prof. Dr. med. Peter Altmeyer, Prof. Dr. med. Martina Bacharach-Buhles

All authors of this article

Last updated on: 03.12.2024

Dieser Artikel auf Deutsch

Definition
This section has been translated automatically.

Collection of regulations for the manufacture of medicinal products, divided into different pharmacopoeias in accordance with §55 of the German Medicinal Products Act (AMG), see classification. The pharmacopoeias contain information on quality, testing, storage, dispensing and designation, as well as recognized pharmaceutical rules.

Classification
This section has been translated automatically.

  • German Pharmacopoeia ( DAB)
  • German Drug Codex ( DAC); see also NRF
  • Pharmacopoea Europaea (Ph. Eur.)
  • Pharmacopoeia of the German Democratic Republic (AB-DDR)
  • Pharmacopoeia for Austria (ÖAB)
  • Pharmacopoea Helvetica (Ph. Helv.)
  • Homeopathic Pharmacopoeia (HAB)
  • British Pharmaceutical Codex (BPC)
  • American Pharmacopoeia (USP)
  • European Pharmacopoeia (Ph. Eur.)

Literature
This section has been translated automatically.

  1. https://www.bfarm.de/DE/Arzneimittel/Zulassung/Zulassungsrelevante-Themen/Arzneibuch/_node.html
  2. Blaschek W (2015) Wichtl tea drugs and phytopharmaceuticals. A handbook for practice. Wissenschaftliche Verlagsgesellschaft Munich. S 37

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Authors

Last updated on: 03.12.2024

Authors: Prof. Dr. med. Peter Altmeyer Prof. Dr. med. Peter Altmeyer Prof. Dr. med. Martina Bacharach-Buhles Prof. Dr. med. Martina Bacharach-Buhles

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