NDC11 85534004900
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 |
|---|---|
| 85534-0049-0 | 85534-0049 |
| 85534-0049-00 | 85534-0049 |
| 85534-049-00 | 85534-049 |
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 |
|---|---|---|---|---|---|---|
| FLUCONAZOLE | FLUCONAZOLE | HAWAII REPACK, INC. | 8aa296e2-ad8d-42f6-8b41-468e2b9cdfb8 | 2026-07-03 | Warnings, Adverse reactions | 85534-0049-0 85534-0049 85534004900 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.