NDC11 72603025401
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 |
|---|---|
| 72603-0254-01 | 72603-0254 |
| 72603-0254-1 | 72603-0254 |
| 72603-254-01 | 72603-254 |
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 |
|---|---|---|---|---|---|---|
| EVEROLIMUS | EVEROLIMUS | NorthStar RxLLC | 5cfca904-b75c-5a39-8cb9-b99bb421bceb | 2024-08-02 | Warnings, Adverse reactions | 72603-254-01 72603-254 72603025401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.