NDC11 71921030956
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 |
|---|---|
| 71921-0309-56 | 71921-0309 |
| 71921-309-56 | 71921-309 |
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 |
|---|---|---|---|---|---|---|
| Varenicline | VARENICLINE TARTRATE | Florida Pharmaceutical Products, LLC | 2b9c8b1e-6193-4d8e-9b50-6aca27294263 | 2024-11-05 | Warnings, Adverse reactions | 71921-309-56 71921-309 71921030956 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.