NDC11 50090739700
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 |
|---|---|
| 50090-7397-0 | 50090-7397 |
| 50090-7397-00 | 50090-7397 |
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 | ATOMOXETINE | A-S Medication Solutions | 793928fb-fbcb-4fc6-90d4-f8a15e6b1f93 | 2024-10-25 | Boxed warning, Warnings, Adverse reactions | 50090-7397-0 50090-7397 50090739700 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.