NDC11 51655019460
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 |
|---|---|
| 51655-0194-60 | 51655-0194 |
| 51655-194-60 | 51655-194 |
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 |
|---|---|---|---|---|---|---|
| Cetirizine | CETIRIZINE HYDROCHLORIDE | Northwind Health Company, LLC | f2b4d221-30ae-5a43-e053-2995a90a238a | 2026-01-01 | Warnings | 51655-194-60 51655-194 51655019460 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.