NDC11 00143987825
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 |
|---|---|
| 00143-9878-25 | 00143-9878 |
| 0143-9878-25 | 0143-9878 |
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 |
|---|---|---|---|---|---|---|
| Cefoxitin | CEFOXITIN | Hikma Pharmaceuticals USA Inc. | d2c449b9-5624-4166-95b1-d7813b3d0445 | 2024-04-11 | Warnings, Adverse reactions | 0143-9878-25 0143-9878 00143987825 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.