NDC11 49884089952
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 |
|---|---|
| 49884-0899-52 | 49884-0899 |
| 49884-899-52 | 49884-899 |
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 sublingual | ZOLPIDEM TARTRATE SUBLINGUAL | Par Health USA, LLC | 44b34e58-114b-4774-9fab-4b188dfe0228 | 2026-04-15 | Boxed warning, Warnings, Adverse reactions | 49884-899-52 49884-899 49884089952 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.