Docket Number:
FDA-2019-D-1536
Issued by:
Guidance Issuing Office
Center for Drug Evaluation and Research

The purpose of this guidance is to describe the benefit-risk assessment framework that the 17 Agency uses in evaluating whether applications for opioid analgesic drugs meet the standard for 18 approval under section 505 of the Federal Food, Drug, and Cosmetic Act. This guidance 19 summarizes the information that should be included in a new drug application for an opioid 20 analgesic drug to facilitate the Agency’s benefit-risk assessment.


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All written comments should be identified with this document's docket number: FDA-2019-D-1536.