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 ?
He added to enhance capacity building of pharmaceutical companies, a number of workshops and training were organized in collaboration with World Health Organization (WHO) and United States Pharmacopoeia in major cities of the country.
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.
12] United States Pharmacopoeia 30 - National Formulary 25 (USP 30 - NF 25), United States Pharmacopeial Convention, Rockville, MD 2007.
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.
The tablets from each lot of the selected formulation F-C meet up the dosage uniformity requirements of United States Pharmacopoeia, USPXXXI as were found unvarying regarding physical dimensions, percent weight variation, percent friability, and percent drug contents (Table- 1).
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).
As the number of products in the vitamin section can be overwhelming, Cohen suggests first looking at the brand, seeking only those committed to science-based protocols for product development, and those that are tested and verified by third-party public health organizations such as the United States Pharmacopoeia (USP).
The analysis was run according to the official methods of United States Pharmacopoeia (USP) for clobetasol propionate (Anon.

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