NDC11 70518003905
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 |
|---|---|
| 70518-0039-05 | 70518-0039 |
| 70518-0039-5 | 70518-0039 |
| 70518-039-05 | 70518-039 |
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 | REMEDYREPACK INC. | ffaf1db4-25a9-48d1-a624-242f9d8e14c7 | 2026-06-22 | Boxed warning, Warnings, Adverse reactions | 70518-0039-5 70518-0039 70518003905 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.