NDC11 60290005503
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 |
|---|---|
| 60290-0055-03 | 60290-0055 |
| 60290-0055-3 | 60290-0055 |
| 60290-055-03 | 60290-055 |
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 |
|---|---|---|---|---|---|---|
| Ranolazine | RANOLAZINE | Umedica Laboratories USA Inc. | a624dc7f-921d-4554-a813-f72dca0133c3 | 2026-08-07 | Warnings, Adverse reactions | 60290-055-03 60290-055 60290005503 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.