NDC11 00069547102
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 |
|---|---|
| 00069-5471-02 | 00069-5471 |
| 00069-5471-2 | 00069-5471 |
| 0069-5471-02 | 0069-5471 |
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 |
|---|---|---|---|---|---|---|
| CEREBYX | FOSPHENYTOIN SODIUM | Pfizer Laboratories Div Pfizer Inc | de5a6711-4abb-4c3d-a18b-266b094ace11 | 2025-05-18 | Boxed warning, Warnings, Adverse reactions | 0069-5471-02 0069-5471 00069547102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.