Business · 06/02/2006Updated: 10/17/2026 · 1 min read
FDA Announces Approval of Labeling Requirements for Prescription Drugs and Biologics
Summary
The U.S. Food and Drug Administration (FDA) has announced that it has received approval from the Office of Management and Budget (OMB) to collect information related to labeling requirements for human prescription drugs and biologics, as mandated by the Paperwork Reduction Act of 1995.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →