JUN 18, 2026 · REGULATORY LABEL UPDATE
FDA supplemental approval: Buprenorphine (REMS)
U.S. Food and Drug Administration
This is an FDA supplemental approval action updating the Risk Evaluation and Mitigation Strategy (REMS) for buprenorphine transdermal film products; it does not report clinical trial efficacy or safety data.
Reported
Approval status date2026-06-18
Submission typeSUPPL (supplement)
Submission classREMS