NDC11 25021011199
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 |
|---|---|
| 25021-0111-99 | 25021-0111 |
| 25021-111-99 | 25021-111 |
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 | Sagent Pharmaceuticals | 4c6f7665-204f-6c69-7669-61204d756e6e | 2020-06-09 | Boxed warning, Warnings, Adverse reactions | 25021-111-99 25021-111 25021011199 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.