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.
FDA supplemental approval for labeling changes to an established epinephrine product; does not report clinical trial outcomes or comparative efficacy data.
FDA supplemental approval of a Risk Evaluation and Mitigation Strategy (REMS) for an oxycodone–acetaminophen combination product; this is a regulatory action, not a clinical efficacy study.