NDC11 59450021101
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 |
|---|---|
| 59450-0211-01 | 59450-0211 |
| 59450-0211-1 | 59450-0211 |
| 59450-211-01 | 59450-211 |
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 (For Women) | MINOXIDIL | Kroger Company | c443fadd-669e-4d29-8b11-ef3c022ca6f4 | 2022-10-25 | Warnings | 59450-211-01 59450-211 59450021101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.