NDC11 72603024601
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 |
|---|---|
| 72603-0246-01 | 72603-0246 |
| 72603-0246-1 | 72603-0246 |
| 72603-246-01 | 72603-246 |
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 |
|---|---|---|---|---|---|---|
| Zileuton | ZILEUTON | NorthStar RxLLC | bc29c998-1324-46aa-8386-e5b2fc9e0b16 | 2024-05-02 | Warnings, Adverse reactions | 72603-246-01 72603-246 72603024601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.