Business · 08/02/2010Updated: 10/17/2026 · 1 min read

FDA Releases Guidance for Industry on Proprietary Names Submission

Summary

The Food and Drug Administration (FDA) has made available a guidance document outlining the requirements for a complete submission to evaluate proprietary names for drugs and biological products, with the aim of preventing medication errors and assessing promotional aspects.

Original source language: Federal Register — Health and Human ServicesOpen original release →

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