NDC11 51662124502
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 |
|---|---|
| 51662-1245-02 | 51662-1245 |
| 51662-1245-2 | 51662-1245 |
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 |
|---|---|---|---|---|---|---|
| ONDANSETRON | ONDANSETRON | HF Acquisition Co LLC, DBA HealthFirst | 768aa02b-8231-5799-e053-2a91aa0a618d | 2024-02-22 | Warnings, Adverse reactions | 51662-1245-2 51662-1245 51662124502 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.