NDC11 70000075301
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 |
|---|---|
| 70000-0753-01 | 70000-0753 |
| 70000-0753-1 | 70000-0753 |
| 70000-753-01 | 70000-753 |
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 | CARDINAL HEALTH 110, LLC. DBA LEADER | 33f9e0de-dff1-4a14-8aec-8c842bf34c31 | 2026-04-13 | Warnings | 70000-0753-1 70000-0753 70000075301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.