Business · 04/12/2014Updated: 10/17/2026 · 1 min read

FDA Releases Draft Guidance for Labeling of Human Prescription Drugs and Biological Products

Summary

The FDA has published a draft guidance to help pharmaceutical companies comply with new labeling requirements for human prescription drugs and biological products, particularly those related to pregnancy, lactation, and reproductive potential.

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

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