NDC11 65862075275
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 |
|---|---|
| 65862-0752-75 | 65862-0752 |
| 65862-752-75 | 65862-752 |
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 | Aurobindo Pharma Limited | 068e6edd-a5fe-40d8-8dcf-ac82b78dced4 | 2024-02-14 | Warnings, Adverse reactions | 65862-752-75 65862-752 65862075275 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.