NDC11 82376600708
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 |
|---|---|
| 82376-6007-08 | 82376-6007 |
| 82376-6007-8 | 82376-6007 |
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 | SPAZI INC. | facdb1c2-c36e-4bcc-a821-f8bad8bb17aa | 2024-01-23 | Warnings | 82376-6007-8 82376-6007 82376600708 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.