NDC11 51655073153
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 |
|---|---|
| 51655-0731-53 | 51655-0731 |
| 51655-731-53 | 51655-731 |
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 |
|---|---|---|---|---|---|---|
| meloxicam | MELOXICAM | Northwind Health Company, LLC | 820f143f-4b0c-4466-be9a-212dab9d984b | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 51655-731-53 51655-731 51655073153 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.