NDC11 51672138903
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 |
|---|---|
| 51672-1389-03 | 51672-1389 |
| 51672-1389-3 | 51672-1389 |
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 |
|---|---|---|---|---|---|---|
| Azelaic Acid | AZELAIC ACID | Sun Pharmaceutical Industries, Inc. | d4e9e95d-1ebd-44df-a91e-59819715659c | 2025-08-22 | Warnings, Adverse reactions | 51672-1389-3 51672-1389 51672138903 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.