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2 developments in the corpus
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JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval of a Risk Evaluation and Mitigation Strategy (REMS) for hydromorphone; this is a regulatory action, not a clinical trial, and does not report efficacy or safety trial outcomes.
JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval of a Risk Evaluation and Mitigation Strategy (REMS) for an existing oxycodone-acetaminophen combination, representing a regulatory action rather than new clinical evidence of efficacy or safety.