NDC11 70518366906
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 |
|---|---|
| 70518-3669-06 | 70518-3669 |
| 70518-3669-6 | 70518-3669 |
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 |
|---|---|---|---|---|---|---|
| prazosin hydrochloride | PRAZOSIN HYDROCHLORIDE | REMEDYREPACK INC. | 95aa9ffb-66bb-4049-a241-0e1166b4c264 | 2026-08-14 | Warnings, Adverse reactions | 70518-3669-6 70518-3669 70518366906 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.