NDC11 55150051005
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 |
|---|---|
| 55150-0510-05 | 55150-0510 |
| 55150-0510-5 | 55150-0510 |
| 55150-510-05 | 55150-510 |
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 |
|---|---|---|---|---|---|---|
| METHOTREXATE | METHOTREXATE | Eugia US LLC | 63bb6fbf-dd59-4edc-af8f-d0c397ca1262 | 2025-07-10 | Boxed warning, Warnings, Adverse reactions | 55150-510-05 55150-510 55150051005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.