NDC11 00069814120
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 |
|---|---|
| 00069-8141-20 | 00069-8141 |
| 0069-8141-20 | 0069-8141 |
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 |
|---|---|---|---|---|---|---|
| Xalkori | CRIZOTINIB | Pfizer Laboratories Div Pfizer Inc | 2a51b0de-47d6-455e-a94c-d2c737b04ff7 | 2025-07-22 | Warnings, Adverse reactions | 0069-8141-20 0069-8141 00069814120 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.