Literature DB >> 14555409

The use of unallowed excipients.

Marshall Steinberg1, Irwin Silverstein.   

Abstract

The laws governing the U.S. Food and Drug Administration (FDA) do not provide for the approval of stand-alone excipients. Current regulations do not permit the use of excipients, but allow their use. The acceptance process for excipients is slow and only recently did the FDA propose draft guidance for nonclinical studies for pharmaceutical excipients. The FDA has made four suggestions to the U.S. Pharmacopoeia concerning including excipient monographs in the National Formulary for excipients not yet allowed. This article reviews these four proposals to identify the proposal that is most appropriate.

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Year:  2003        PMID: 14555409     DOI: 10.1177/109158180302200506

Source DB:  PubMed          Journal:  Int J Toxicol        ISSN: 1091-5818            Impact factor:   2.032


  2 in total

1.  Identification of phthalates in medications and dietary supplement formulations in the United States and Canada.

Authors:  Katherine E Kelley; Sonia Hernández-Díaz; Erica L Chaplin; Russ Hauser; Allen A Mitchell
Journal:  Environ Health Perspect       Date:  2011-12-15       Impact factor: 9.031

2.  Excipient Innovation Through Precompetitive Research.

Authors:  Yihua Bruce Yu; Marc B Taraban; Katharine T Briggs; Robert G Brinson; John P Marino
Journal:  Pharm Res       Date:  2021-12-20       Impact factor: 4.580

  2 in total

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