NDC11 51672140204
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 |
|---|---|
| 51672-1402-04 | 51672-1402 |
| 51672-1402-4 | 51672-1402 |
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 |
|---|---|---|---|---|---|---|
| Calcipotriene and Betamethasone Dipropionate | CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE | Sun Pharmaceutical Industries, Inc. | 1d0ab2e6-1ab1-4d3e-ad55-7fa26446f191 | 2025-07-01 | Warnings, Adverse reactions | 51672-1402-4 51672-1402 51672140204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.