NDC11 59726001253
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 |
|---|---|
| 59726-0012-53 | 59726-0012 |
| 59726-012-53 | 59726-012 |
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 |
|---|---|---|---|---|---|---|
| Arthritis Pain Reliever | DICLOFENAC SODIUM | P & L Development, LLC | 2596645a-b736-4d3c-82a0-00713f1b6fbd | 2022-12-15 | Warnings | 59726-012-53 59726-012 59726001253 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.