NDC11 59651051105
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 |
|---|---|
| 59651-0511-05 | 59651-0511 |
| 59651-0511-5 | 59651-0511 |
| 59651-511-05 | 59651-511 |
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 | Aurobindo Pharma Limited | cc344f7c-0eb3-4e63-a09e-b682acca2bb5 | 2026-07-23 | Boxed warning, Warnings, Adverse reactions | 59651-511-05 59651-511 59651051105 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.