NDC11 53489038705
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 |
|---|---|
| 53489-0387-05 | 53489-0387 |
| 53489-0387-5 | 53489-0387 |
| 53489-387-05 | 53489-387 |
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 |
|---|---|---|---|---|---|---|
| MINOXIDIL | MINOXIDIL | Sun Pharmaceutical Industries, Inc. | 0354a7f5-5917-44dc-9963-411104008cb5 | 2026-02-09 | Boxed warning, Warnings, Adverse reactions | 53489-387-05 53489-387 53489038705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.