NDC11 71335098100
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 |
|---|---|
| 71335-0981-0 | 71335-0981 |
| 71335-0981-00 | 71335-0981 |
| 71335-981-00 | 71335-981 |
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 | Bryant Ranch Prepack | 4e9e945d-5ffc-48de-99fa-3fb36c5bc2b9 | 2024-05-30 | Boxed warning, Warnings, Adverse reactions | 71335-0981-0 71335-0981 71335098100 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.