NDC11 40032099905
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 |
|---|---|
| 40032-0999-05 | 40032-0999 |
| 40032-0999-5 | 40032-0999 |
| 40032-999-05 | 40032-999 |
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 |
|---|---|---|---|---|---|---|
| cevimeline hydrochloride | CEVIMELINE HYDROCHLORIDE | Novel Laboratories, Inc. | d7432a48-1142-431e-997f-8419dc724824 | 2016-02-09 | Warnings, Adverse reactions | 40032-999-05 40032-999 40032099905 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.