NDC11 71921022206
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 |
|---|---|
| 71921-0222-06 | 71921-0222 |
| 71921-0222-6 | 71921-0222 |
| 71921-222-06 | 71921-222 |
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 |
|---|---|---|---|---|---|---|
| Lacosamide | LACOSAMIDE | Florida Pharmaceutical Products, LLC | 3680c0ff-7f5c-4572-b1eb-4fea96b7fbe2 | 2025-02-12 | Warnings, Adverse reactions | 71921-222-06 71921-222 71921022206 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.