NDC11 00591333119
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 |
|---|---|
| 00591-3331-19 | 00591-3331 |
| 0591-3331-19 | 0591-3331 |
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 XL | BUPROPION HYDROCHLORIDE | Actavis Pharma, Inc. | a1e768fd-c28f-4b49-822d-ccc315b4099c | 2026-07-16 | Boxed warning, Warnings, Adverse reactions | 0591-3331-19 0591-3331 00591333119 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.