Business · 16/05/2007Updated: 10/17/2026 · 1 min read
FDA Releases Draft Guidance on Labeling for Human Prescription Drugs
Summary
The Food and Drug Administration (FDA) has released a draft guidance document to help pharmaceutical companies and FDA reviewers determine the established pharmacologic class for human prescription drugs and select the correct term for labeling purposes.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →