FDAsafety guidance66% confidence
FDA AP — OXYCONTIN (SUPPL)
Source: FDA
Why This Matters
Why this matters: sets a safety guidance precedent in the same sub-indication (pain) as KNOA Pharma; the same agency is already in play for this signal, so precedent weight is higher.
Regulatory Analysis
Application NDA022272. Sponsor: KNOA PHARMA. Submission status: AP. Submission type: SUPPL. Review priority: N/A. Active ingredients: OXYCODONE HYDROCHLORIDE.
Supporting Context
- Therapeutic area
- Pain Management · Opioid
- Sub-indication
- Pain
Related signal: FDA Accepts Supplemental Application for OxyContin by KNOA Pharma