NDC11 51672424602
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 |
|---|---|
| 51672-4246-02 | 51672-4246 |
| 51672-4246-2 | 51672-4246 |
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 |
|---|---|---|---|---|---|---|
| doxepin hydrochloride | DOXEPIN HYDROCHLORIDE | Sun Pharmaceutical Industries, Inc. | 554ab06f-6420-42b3-89d1-d97554c237d8 | 2025-08-06 | Warnings, Adverse reactions | 51672-4246-2 51672-4246 51672424602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.