NDC11 51672136202
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 |
|---|---|
| 51672-1362-02 | 51672-1362 |
| 51672-1362-2 | 51672-1362 |
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 |
|---|---|---|---|---|---|---|
| Naftifine Hydrochloride | NAFTIFINE HYDROCHLORIDE | Sun Pharmaceutical Industries, Inc. | d50961c2-e97f-4583-91d6-7cafd25a8c3d | 2025-07-07 | Warnings, Adverse reactions | 51672-1362-2 51672-1362 51672136202 |