NDC11 43386043105
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 |
|---|---|
| 43386-0431-05 | 43386-0431 |
| 43386-0431-5 | 43386-0431 |
| 43386-431-05 | 43386-431 |
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 | Lupin Pharmaceuticals,Inc. | 801cb437-c189-44f5-83eb-a51c365d8a6b | 2024-01-30 | Boxed warning, Warnings, Adverse reactions | 43386-431-05 43386-431 43386043105 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.