NDC11 51991098101
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 |
|---|---|
| 51991-0981-01 | 51991-0981 |
| 51991-0981-1 | 51991-0981 |
| 51991-981-01 | 51991-981 |
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 | Breckenridge Pharmaceutical, Inc. | cbda91f7-4411-4016-80d6-0a349931956d | 2026-08-26 | Boxed warning, Warnings, Adverse reactions | 51991-981-01 51991-981 51991098101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.