NDC11 69729012324
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 |
|---|---|
| 69729-0123-24 | 69729-0123 |
| 69729-123-24 | 69729-123 |
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 |
|---|---|---|---|---|---|---|
| PROXEN NP 660 | NAPROXEN SODIUM | OPMX LLC | 09990b2f-202e-b4df-e063-6394a90a055b | 2023-12-27 | Warnings | 69729-123-24 69729-123 69729012324 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.