NDC11 51672200102
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 |
|---|---|
| 51672-2001-02 | 51672-2001 |
| 51672-2001-2 | 51672-2001 |
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 |
|---|---|---|---|---|---|---|
| Miconazole Nitrate | MICONAZOLE NITRATE | Sun Pharmaceutical Industries, Inc. | 7fd4037e-d350-47b7-a7d9-a43b8e366fa0 | 2026-08-25 | Warnings | 51672-2001-2 51672-2001 51672200102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.