NDC11 80425006102
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 |
|---|---|
| 80425-0061-02 | 80425-0061 |
| 80425-0061-2 | 80425-0061 |
| 80425-061-02 | 80425-061 |
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 |
|---|---|---|---|---|---|---|
| Zolpidem Tartrate | ZOLPIDEM TARTRATE | Advanced Rx of Tennessee, LLC | af87df4e-2c97-e23e-e053-2a95a90ab354 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 80425-0061-2 80425-0061 80425006102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.