NDC11 57483016513
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 |
|---|---|
| 57483-0165-13 | 57483-0165 |
| 57483-165-13 | 57483-165 |
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 |
|---|---|---|---|---|---|---|
| REGOXIDINE (FOR MEN) | MINOXIDIL | INNOVUS PHARMACEUTICALS, INC. | d191b3a9-0fb7-45cc-82a1-b64a79c0c125 | 2026-01-20 | Warnings | 57483-165-13 57483-165 57483016513 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.