Drug or technology
11 developments in the corpus
Following this puts new work involving it at the top of your briefing, with a note saying why it is there. Links are taken from the source record, never inferred.
Latest
Everything in the corpus, newest first.
JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval of a Risk Evaluation and Mitigation Strategy (REMS) for OxyContin; this is a regulatory action, not a clinical study, and does not report efficacy or comparative 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 oxycodone hydrochloride tablets; 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
This is an FDA supplemental approval action for a Risk Evaluation and Mitigation Strategy (REMS) requirement for oxycodone hydrochloride tablets; it is a regulatory record, not a clinical trial, and does not report efficacy or safety outcome data.
JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval action for oxycodone hydrochloride oral solution under REMS framework; describes regulatory status, not clinical efficacy or safety data.
JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval of oxycodone hydrochloride oral solution under REMS framework; regulatory action, not efficacy evidence.
JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval of an oxycodone hydrochloride formulation under REMS; a regulatory action that does not itself report clinical trial outcomes or comparative efficacy.
JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval of an opioid formulation under REMS requirements; this is a regulatory action, not a clinical evidence evaluation.
JUN 18, 2026 · REGULATORY LABEL UPDATE
U.S. Food and Drug Administration
FDA supplemental approval action for oxycodone hydrochloride oral solution under REMS requirements; this is a regulatory classification change, not a clinical efficacy finding.