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Volume 350:2327-2329 June 3, 2004 Number 23 Next

	Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

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The proposal to switch levonorgestrel emergency contraception (sold under the brand name Plan B) to over-the-counter status in the United States is in limbo. In May, the Food and Drug Administration (FDA) rejected the application of Barr Pharmaceuticals for nonprescription sales of Plan B. Dr. Steven Galson, the acting director of the FDA's Center for Drug Evaluation and Research, wrote that the company had "not provided adequate data to support a conclusion that Plan B can be used safely by young adolescent women for emergency contraception without the professional supervision of a practitioner licensed by law to administer the drug." . . . [Full Text of this Article]

Related Letters:

Plan B — The FDA and Emergency Contraception
Schwarz E. B.
Extract | Full Text | PDF  
N Engl J Med 2004; 351:1031-1032, Sep 2, 2004. Correspondence

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