NDC11 70518274902
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 |
|---|---|
| 70518-2749-02 | 70518-2749 |
| 70518-2749-2 | 70518-2749 |
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 |
|---|---|---|---|---|---|---|
| CEFIXIME | CEFIXIME | REMEDYREPACK INC. | d6718f02-8eea-4c2f-9aa2-65121d9a6e4c | 2026-07-28 | Warnings, Adverse reactions | 70518-2749-2 70518-2749 70518274902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.