NDC11 53345001401
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 |
|---|---|
| 53345-0014-01 | 53345-0014 |
| 53345-0014-1 | 53345-0014 |
| 53345-014-01 | 53345-014 |
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 | 50bab3b2-f710-46ff-96cd-1ec4d4658529 | 2019-11-22 | Warnings | 53345-014-01 53345-014 53345001401 |
| Ibuprofen | IBUPROFEN | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | 58bff8bf-5a4e-4390-9c03-e266d31deb6b | 2019-11-22 | Warnings | 53345-014 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.