NDC11 55150024747
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 |
|---|---|
| 55150-0247-47 | 55150-0247 |
| 55150-247-47 | 55150-247 |
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 |
|---|---|---|---|---|---|---|
| Levetiracetam | LEVETIRACETAM IN SODIUM CHLORIDE | Eugia US LLC | e5eb4c89-8ee9-4474-9cb1-c3b3dc262a4a | 2024-04-01 | Warnings, Adverse reactions | 55150-247-47 55150-247 55150024747 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.