NDC11 00069083038
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 |
|---|---|
| 00069-0830-38 | 00069-0830 |
| 00069-830-38 | 00069-830 |
| 0069-0830-38 | 0069-0830 |
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 |
|---|---|---|---|---|---|---|
| SUTENT | SUNITINIB MALATE | Pfizer Laboratories Div Pfizer Inc | 43a4d7f8-48ae-4a63-9108-2fa8e3ea9d9c | 2026-02-20 | Boxed warning, Warnings, Adverse reactions | 0069-0830-38 0069-0830 00069083038 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.