Medscape

Introduction to the New Prescription Drug Labeling by the Food and Drug Administration

Purpose: The revised prescription drug labeling developed by the Food and Drug Administration (FDA) is described. Summary: A new FDA final rule, "Requirements on Content and Format of Labeling for ...

Research: FDA drug labels not proof of patent violation

Federal law requires every prescription drug to include a document describing dosing guidelines, contraindications, results ...
MD&M East

FDA Stops Issuing NHRIC and NDC Codes for Devices

FDA says that to conform to change made under the Unique Device Identification (UDI) final rule, it has stopped issuing National Health Related Items Code (NHRIC) and National Drug Code (NDC) labeler ...
ascopubs.org

Patient-Reported Outcomes Labeling for Products Approved by the Office of Hematology and Oncology Products of the US Food and Drug Administration (2010-2014)

Randomized Controlled Trial of Family Therapy in Advanced Cancer Continued Into Bereavement FDA Drug Approval Reports by Month were reviewed to obtain the number of new molecular entities and biologic ...