NDC11 00591037001
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 |
|---|---|
| 00591-0370-01 | 00591-0370 |
| 00591-0370-1 | 00591-0370 |
| 00591-370-01 | 00591-370 |
| 0591-0370-01 | 0591-0370 |
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 |
|---|---|---|---|---|---|---|
| Loxapine | LOXAPINE | Actavis Pharma, Inc. | a6107bb1-3e23-4c5d-bbf4-5e29deff6728 | 2025-03-31 | Boxed warning, Warnings, Adverse reactions | 0591-0370-01 0591-0370 00591037001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.