Pfizer Takes Action Against Generics At FDA

Law360 (February 8, 2006, 12:00 AM EST) -- Generic versions of Pfizer Inc.’s antibiotic Zithromax made by Teva Pharmaceuticals U.S.A. and Novartis subsidiary Sandoz Inc. do not accurately describe the drugs' active ingredients and are a danger to consumers, according to petition filed by Pfizer with the U.S. Food and Drug Administration Wednesday.

The petition is the latest in a series of maneuvers that have targeted the generic companies’ at-risk launch of the drug, which the FDA approved for generic manufacture in November 2005. The main patent for Zithromax expired on Nov. 1, although...
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