NDC11 85534008000
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 |
|---|---|
| 85534-0080-0 | 85534-0080 |
| 85534-0080-00 | 85534-0080 |
| 85534-080-00 | 85534-080 |
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 |
|---|---|---|---|---|---|---|
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | HAWAII REPACK, INC. | 7fb0f56e-c098-49e4-b075-2eb8936582aa | 2026-07-13 | Warnings, Adverse reactions | 85534-0080-0 85534-0080 85534008000 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.