Business · 02/07/2019Updated: 10/17/2026 · 1 min read
FDA Releases Draft Guidance on Labeling for Human Prescription Drugs and Biological Products
Summary
The FDA has released a draft guidance to help pharmaceutical companies write clear and consistent labeling for human prescription drugs and biological products, addressing drug abuse and dependence.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →