NDC11 53345003902
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 |
|---|---|
| 53345-0039-02 | 53345-0039 |
| 53345-0039-2 | 53345-0039 |
| 53345-039-02 | 53345-039 |
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 |
|---|---|---|---|---|---|---|
| Ibuprofen | IBUPROFEN | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | f42506f7-896c-47a9-a4b1-ed72434d7aa0 | 2019-11-22 | Warnings | 53345-039-02 53345-039 53345003902 |
| Ibuprofen | IBUPROFEN | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | daf579dc-91d1-4950-b637-c1a34f5542c5 | 2019-11-22 | Warnings | 53345-039 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.