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Dietary Supplement and Nonprescription Drug Consumer Protection Act (P.L. 109-462).

Summarizes provisions of P.L. 109-462, the Dietary Supplement and Nonprescription Drug Consumer Protection Act of 2006, which requires manufacturers of dietary supplements and over-the-counter drugs to report serious adverse events to the FDA, including deaths, birth defects, hospitalizations, incap...

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Bibliographic Details
Corporate Authors:	Library of Congress. Congressional Research Service, ProQuest (Firm)
Format:	eBook
Language:	English
Published:	[Place of publication not identified] : [publisher not identified], 2007.
Series:	U.S. Congressional Research.
Subjects:	People with disabilities. Medical laws and legislation. Pharmaceutical industry. Electronic books.
Online Access:	Connect to the full text of this electronic book

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