NDC11 80425004301
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 |
|---|---|
| 80425-0043-01 | 80425-0043 |
| 80425-0043-1 | 80425-0043 |
| 80425-043-01 | 80425-043 |
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 | Advanced Rx of Tennessee, LLC | af9d0426-9cbb-a6a3-e053-2995a90aed2f | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 80425-0043-1 80425-0043 80425004301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.