NDC11 53345004201
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 |
|---|---|
| 53345-0042-01 | 53345-0042 |
| 53345-0042-1 | 53345-0042 |
| 53345-042-01 | 53345-042 |
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 |
|---|---|---|---|---|---|---|
| NAPROXEN SODIUM | NAPROXEN SODIUM | Humanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd | 1d5981dd-e3f5-48a3-a5f1-ce49689cdfac | 2019-11-08 | Warnings | 53345-042-01 53345-042 53345004201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.