# Determination That SANOREX (Mazindol) Tablets 1 and 2 Milligrams Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness; Correction
**AGENCY:**
Food and Drug Administration. HHS.
**ACTION:**
Notice; correction.
**SUMMARY:**
The Food and Drug Administration is correcting a notice that appeared in the *Federal Register* of July 15, 2008 (73 FR 40582). The document announced the determination that SANOREX (mazindol) Tablets, 1 and 2 milligrams (mg), were not withdrawn from sale for reasons of safety or effectiveness. The document was published with an incorrect docket number. This document corrects that error.
**FOR FURTHER INFORMATION CONTACT:**
Joyce Strong, Office of Policy and Planning (HF-27), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-7010.
**SUPPLEMENTARY INFORMATION:**
In FR Doc. E8-15998, appearing on page 40582 in the *Federal Register* of Tuesday, July 15, 2008, the following correction is made:
1. On page 40582, in the third column, in the headings section of the document, “[Docket No. FDA-2007-P-0326]” is corrected to read “[Docket No. FDA-2007-P-0300] (formerly 2007P-0326)”.
Dated: July 22, 2008.
Jeffrey Shuren,
Associate Commissioner for Policy and Planning.