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FDA

Regulatory intelligence
FDAsafety guidance66% confidence

FDA AP — ROXYBOND (SUPPL)

Source: FDA

Why This Matters

Why this matters: sets a safety guidance precedent in the same sub-indication (pain) as Protega Pharmaceuticals; the same agency is already in play for this signal, so precedent weight is higher.

Regulatory Analysis

Application NDA209777. Sponsor: PROTEGA PHARMS. 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 Supplement Application for RoxyBond (NDA209777)

Source

View source document

Related Signal

Open signal — FDA Accepts Supplement Application for RoxyBond (NDA209777)
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