NDC11 50268005911
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 |
|---|---|
| 50268-0059-11 | 50268-0059 |
| 50268-059-11 | 50268-059 |
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 |
|---|---|---|---|---|---|---|
| Atomoxetine Hydrochloride | ATOMOXETINE HYDROCHLORIDE | AvPAK | a9df4617-b406-70ba-e053-2995a90a28e8 | 2025-12-09 | Boxed warning, Warnings, Adverse reactions | 50268-059-11 50268-059 50268005911 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.