NDC11 00037682315
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 |
|---|---|
| 00037-6823-15 | 00037-6823 |
| 0037-6823-15 | 0037-6823 |
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 |
|---|---|---|---|---|---|---|
| PROCTOFOAM NS | PRAMOXINE HYDROCHLORIDE | Viatris Specialty LLC | cddc8d81-21b8-11e4-8c21-0800200c9a66 | 2025-08-15 | Warnings | 0037-6823-15 0037-6823 00037682315 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.