NDC11 62559016701
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 62559-0167-01 | 62559-0167 |
| 62559-0167-1 | 62559-0167 |
| 62559-167-01 | 62559-167 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Oxycodone Hydrochloride | OXYCODONE HYDROCHLORIDE | ANI Pharmaceuticals, Inc. | 5df92fed-6194-4905-9ef2-9eed0d2e8086 | 2026-01-22 | Boxed warning, Warnings, Adverse reactions | 62559-167-01 62559-167 62559016701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.