NDC11 73473080001
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 |
|---|---|
| 73473-0800-01 | 73473-0800 |
| 73473-0800-1 | 73473-0800 |
| 73473-800-01 | 73473-800 |
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 |
|---|---|---|---|---|---|---|
| DICYCLOMINE HYDROCHLORIDE | DICYCLOMINE HYDROCHLORIDE | Solaris Pharma Corporation | 4237bb2e-d6dd-4e3a-baa2-85be5dc3c8f2 | 2025-07-03 | Warnings, Adverse reactions | 73473-800-01 73473-800 73473080001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.