NDC11 85534000603
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 |
|---|---|
| 85534-0006-03 | 85534-0006 |
| 85534-0006-3 | 85534-0006 |
| 85534-006-03 | 85534-006 |
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 |
|---|---|---|---|---|---|---|
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | HAWAII REPACK, INC. | b4a1d3b8-afcf-47e3-96d3-469d8f408a31 | 2025-06-11 | Boxed warning, Warnings, Adverse reactions | 85534-0006-3 85534-0006 85534000603 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.