NDC11 43063027304
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 |
|---|---|
| 43063-0273-04 | 43063-0273 |
| 43063-0273-4 | 43063-0273 |
| 43063-273-04 | 43063-273 |
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 | PD-Rx Pharmaceuticals, Inc. | d117de5f-64e5-464c-b782-de0f07e66c8e | 2026-01-20 | Warnings, Adverse reactions | 43063-273-04 43063-273 43063027304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.