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Business · 15/04/2016Updated: 10/17/2026 · 1 min read

FDA Corrects Withdrawal of Propoxyphene Drug Approval, Includes Xanodyne Pharmaceuticals

Summary

The FDA is correcting a notice that withdrew approval of 8 new drug applications and 46 abbreviated new drug applications for prescription pain medications containing propoxyphene, including a mistake that left Xanodyne Pharmaceuticals' NDA 017507 still approved

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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