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USP IDENTITY STANDARDS FOR 23 OTC INGREDIENTS

This article was originally published in The Tan Sheet

Executive Summary

USP IDENTITY STANDARDS FOR 23 OTC INGREDIENTS may be developed with the help of industry, based on interest expressed by members of the Nonprescription Drug Manufacturers Association, NDMA said in a recent letter to FDA. NDMA noted that after surveying its members on whether they would be interested in assisting the U.S. Pharmacopeia in developing identity standards for 55 OTC ingredients that lack them, companies responded affirmatively for 22 ingredients that are currently listed in tentative final monographs and for one ingredient that is listed in a final monograph, chlorophyllin copper complex.

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