NDC11 80425007301
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 |
|---|---|
| 80425-0073-01 | 80425-0073 |
| 80425-0073-1 | 80425-0073 |
| 80425-073-01 | 80425-073 |
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 ODT | ONDANSETRON | Advanced Rx of Tennessee, LLC | af836a30-5e51-5c97-e053-2995a90a15b9 | 2024-12-31 | Warnings, Adverse reactions | 80425-0073-1 80425-0073 80425007301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.