State Release 153
Guidance for : Clarification of NDC Requirement for Physician-Administered Drugs Section 6002 of the Deficit Reduction Act (DRA) and 42 CFR Part 447.520 set conditions for States to obtain FFP for physician-administered drugs. States must collect National Drug Codes (NDCs) on claims submitted for physician-administered drugs in order for the States to bill manufacturers for rebates.
Issued by: Centers for Medicare & Medicaid Services (CMS)
Issue Date: October 16, 2009
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.