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U.S. Dept. of Health & Human Services
Formulary Reference File Frequently Asked Questions
Guidance for frequently asked questions pertain to CMS’ Formulary Reference File (FRF). The FRF serves as a listing of drug products that can be included on Part D sponsors’ Health Plan Management System (HPMS) formulary files that are submitted to CMS for review and approval.
Issued by: Centers for Medicare & Medicaid Services (CMS)
Issue Date: April 08, 2014
HHS is committed to making its websites and documents accessible to the widest possible audience, including individuals with disabilities. We are in the process of retroactively making some documents accessible. If you need assistance accessing an accessible version of this document, please reach out to the guidance@hhs.gov.
DISCLAIMER: The contents of this database lack the force and effect of law, except as authorized by law (including Medicare Advantage Rate Announcements and Advance Notices) or as specifically incorporated into a contract. The Department may not cite, use, or rely on any guidance that is not posted on the guidance repository, except to establish historical facts.
Date Published: 6/4/2021
