United States Pharmacopoeia

United States Pharmacopoeia,

n.pr 1., the nongovernmental organization that promotes public health and safety by establishing state-of-the-art standards for medications. Also called
USP-NF. 2., the reference work published by this organization in which these standards may be found. In this context, it is more properly known as the
United States Pharmacopoeia and the
National Formulary.
References in periodicals archive ?
United States Pharmacopoeia (USP) and Japanese Pharmacopoeia Excipients (JPE) and will be part of Merck Millipore's Emprove[sup.
The Oxygen Gas Produced By The Oxygen Generator Shall Meet The United States Pharmacopoeia (usp) Specification For Oxygen 95 Percent, 17th Edition, 1997.
A recent United States Pharmacopoeia (USP) stimulus to the revision process paper (1) has taken a life cycle approach to the development, validation and use of analytical procedures.
Moreover, these grades are fully tested in accordance with the relevant European Pharmacopoeia (EP) and United States Pharmacopoeia (USP) requirements to meet the needs in the pharmaceutical industry for an optimal quality and safety for their packaged drug products during shelf-life.
He is a member of the United States Pharmacopoeia 2010-2015 Convention, Editorial Board Chair of AOAC International, and is an advisory board member of the American Botanical Council and the American Herbal Pharmacopeia.
Finally it was listed in both the United States Pharmacopoeia (USP) from 1820-1936 and the British Herbal Pharmacopeia (BHP) in 1867 and then in the European Scientific Cooperative of Phytotherapy in 1996.
The assay of amodiaquine tablets in the artesunate/ amodiaquine combi-packs was performed according to the United States Pharmacopoeia procedure (19).
The analysis was run according to the official methods of United States Pharmacopoeia (USP) for clobetasol propionate (Anon.
10] United states pharmacopoeia, USP-27; NF 22 the national formulary official from January 1, 2004.
We also test for compliance to United States Pharmacopoeia (USP Class VI) and to ISO 10993 as required, and will supply certifications as necessary.
The food industry consumes various grades of Riboflavin including highly pure powder forms which meet the monograph requirements of the United States Pharmacopoeia (USP) and the Food Chemicals Codex (FCC).
Estriol has a longstanding United States Pharmacopoeia monograph, an accepted standard for drug ingredients absent significant health risks.

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