NDC11 00024590200
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 |
|---|---|
| 00024-5902-0 | 00024-5902 |
| 00024-5902-00 | 00024-5902 |
| 0024-5902-00 | 0024-5902 |
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 |
|---|---|---|---|---|---|---|
| Praluent | ALIROCUMAB | Sanofi-Aventis U.S. LLC | 446f6b5c-0dd4-44ff-9bc2-c2b41f2806b4 | 2026-07-07 | Warnings, Adverse reactions | 0024-5902-00 0024-5902 00024590200 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.