NDC11 72722010305
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 |
|---|---|
| 72722-0103-05 | 72722-0103 |
| 72722-0103-5 | 72722-0103 |
| 72722-103-05 | 72722-103 |
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 | The ACME Laboratories Ltd. | 5679ed64-8424-4e63-a3c9-91d80fff2ca6 | 2026-03-04 | Boxed warning, Warnings, Adverse reactions | 72722-103-05 72722-103 72722010305 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.