NDC11 87722009201
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 |
|---|---|
| 87722-0092-01 | 87722-0092 |
| 87722-0092-1 | 87722-0092 |
| 87722-092-01 | 87722-092 |
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 |
|---|---|---|---|---|---|---|
| apgwgzminoxidil5% | MINOXIDIL | Guangdong Jiaoyu Biotechnology Co., Ltd | 596d0b43-5cb1-be25-e063-6394a90abbed | 2026-08-19 | Warnings | 87722-092-01 87722-092 87722009201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.