NDC11 68682058130
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 |
|---|---|
| 68682-0581-30 | 68682-0581 |
| 68682-581-30 | 68682-581 |
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 Hydrobromide | BUPROPION HYDROBROMIDE | Oceanside Pharmaceuticals | 3ec04240-baef-44d7-8d73-a181171eec43 | 2026-06-01 | Boxed warning, Warnings, Adverse reactions | 68682-581-30 68682-581 68682058130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.