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Food and Drug Administration

Endocrinologic and Metabolic Drugs Advisory Committee

June 13, 2007


NDA 21-888

ZIMULTI® (rimonabant) – Sanofi-Aventis


The statements contained in this document(s) are those of the product's sponsor, not FDA, and FDA does not necessarily agree with the sponsor's statements. FDA has not made a final determination about the safety or effectiveness of the product described in this document.

Sanofi-Aventis Briefing Document (pdf(html)



Portions of this document have been determined to be exempt from disclosure under the Freedom of Information Act (the FOIA) (5 U.S.C. §552). These redacted portions will appear as white space on the screen or on the printed page.

FDA Briefing Document (pdf)

Bibliography Addendum (pdf)


Page last updated June 11, 2007 kkhorizonal rule
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