NDC11 43386076130
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 |
|---|---|
| 43386-0761-30 | 43386-0761 |
| 43386-761-30 | 43386-761 |
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 | Lupin Pharmaceuticals,Inc. | 6db679f6-b1f8-4fbf-9e87-9cef4650c45a | 2020-11-18 | Boxed warning, Warnings, Adverse reactions | 43386-761-30 43386-761 43386076130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.