NDC11 80425059301
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 |
|---|---|
| 80425-0593-01 | 80425-0593 |
| 80425-0593-1 | 80425-0593 |
| 80425-593-01 | 80425-593 |
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 |
|---|---|---|---|---|---|---|
| Ramelteon | RAMELTEON | Advanced Rx of Tennessee, LLC | 57b24572-f601-b092-e063-6394a90afa53 | 2026-07-27 | Warnings, Adverse reactions | 80425-0593-1 80425-0593 80425059301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.