NDC11 70069082001
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 |
|---|---|
| 70069-0820-01 | 70069-0820 |
| 70069-0820-1 | 70069-0820 |
| 70069-820-01 | 70069-820 |
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 |
|---|---|---|---|---|---|---|
| HYDROXYUREA | HYDROXYUREA | Somerset Therapeutics, LLC | 9752a347-b42c-44d5-8fd1-c538f7f239dc | 2024-09-23 | Warnings, Adverse reactions | 70069-820-01 70069-820 70069082001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.