NDC11 51655096752
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 |
|---|---|
| 51655-0967-52 | 51655-0967 |
| 51655-967-52 | 51655-967 |
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 |
|---|---|---|---|---|---|---|
| Alfuzosin hydrochloride | ALFUZOSIN HYDROCHLORIDE | Northwind Health Company, LLC | ffbd22eb-9df5-e0ad-e053-6294a90a7d4e | 2026-01-01 | Warnings, Adverse reactions | 51655-967-52 51655-967 51655096752 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.