NDC11 53489015702
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 |
|---|---|
| 53489-0157-02 | 53489-0157 |
| 53489-0157-2 | 53489-0157 |
| 53489-157-02 | 53489-157 |
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 |
|---|---|---|---|---|---|---|
| Allopurinol | ALLOPURINOL | Sun Pharmaceutical Industries, Inc. | fd8f8b8b-f25e-46e9-969a-65363b66e09b | 2026-07-31 | Warnings, Adverse reactions | 53489-157-02 53489-157 53489015702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.