NDC11 63941024503
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 |
|---|---|
| 63941-0245-03 | 63941-0245 |
| 63941-0245-3 | 63941-0245 |
| 63941-245-03 | 63941-245 |
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 |
|---|---|---|---|---|---|---|
| All Day Pain Relief | NAPROXEN SODIUM | VALU MERCHANDISERS COMPANY | 593b915f-045a-40b7-b86e-0d1cb41f2bb8 | 2024-12-04 | Warnings | 63941-245-03 63941-245 63941024503 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.