NDC11 51672401601
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 |
|---|---|
| 51672-4016-01 | 51672-4016 |
| 51672-4016-1 | 51672-4016 |
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 |
|---|---|---|---|---|---|---|
| Etodolac | ETODOLAC | Sun Pharmaceutical Industries, Inc. | ec82b108-6a6f-4d1b-82cb-831d4ed36c80 | 2026-07-15 | Boxed warning, Warnings, Adverse reactions | 51672-4016-1 51672-4016 51672401601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.