NDC11 00069080901
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 |
|---|---|
| 00069-0809-01 | 00069-0809 |
| 00069-0809-1 | 00069-0809 |
| 00069-809-01 | 00069-809 |
| 0069-0809-01 | 0069-0809 |
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 |
|---|---|---|---|---|---|---|
| INFLECTRA | INFLIXIMAB-DYYB | Pfizer Laboratories Div Pfizer Inc | 37eaca10-d812-48bc-8b8e-b836bfa9968f | 2026-07-28 | Boxed warning, Warnings, Adverse reactions | 0069-0809-01 0069-0809 00069080901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.