FDAsafety guidance66% confidence
FDA AP — SELEXIPAG (ORIG)
Source: FDA
Why This Matters
Why this matters: sets a safety guidance precedent in the same sub-indication (cardiology) as Actelion; the same agency is already in play for this signal, so precedent weight is higher.
Regulatory Analysis
Application ANDA214055. Sponsor: RK PHARMA. Submission status: AP. Submission type: ORIG. Review priority: STANDARD. Active ingredients: SELEXIPAG.
Supporting Context
- Therapeutic area
- Pulmonary Arterial Hypertension · Oral Therapy
- Sub-indication
- Hypertension
Related signal: FDA Accepts Supplemental Application for UPTRAVI (Selexipag)