NDC11 87837000101
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 |
|---|---|
| 87837-0001-01 | 87837-0001 |
| 87837-0001-1 | 87837-0001 |
| 87837-001-01 | 87837-001 |
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 |
|---|---|---|---|---|---|---|
| 5%MINOXIDIL TOPICAL FOAM | MINOXIDIL | Veloce Trading Co., Limited | 56f87881-653f-17e6-e063-6294a90a6787 | 2026-07-19 | Warnings | 87837-001-01 87837-001 87837000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.