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 labeling approval for an existing combination product; regulatory action that does not contain clinical trial data or efficacy evidence.
FDA supplemental labeling approval for Qtern (dapagliflozin/saxagliptin); indicates label modification without new efficacy or safety trial data reported here.