NDC11 00781531501
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 |
|---|---|
| 00781-5315-01 | 00781-5315 |
| 00781-5315-1 | 00781-5315 |
| 0781-5315-01 | 0781-5315 |
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 | Sandoz Inc | b1b0085f-d9fe-430a-9bd5-607f607bf7e1 | 2024-06-03 | Boxed warning, Warnings, Adverse reactions | 0781-5315-01 0781-5315 00781531501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.