NDC11 51672131506
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 |
|---|---|
| 51672-1315-06 | 51672-1315 |
| 51672-1315-6 | 51672-1315 |
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 |
|---|---|---|---|---|---|---|
| Mometasone Furoate | MOMETASONE FUROATE | Sun Pharmaceutical Industries, Inc. | ce61920d-65df-4423-925d-091e624ea32e | 2025-07-07 | Warnings, Adverse reactions | 51672-1315-6 51672-1315 51672131506 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.