NDC11 87338098300
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 |
|---|---|
| 87338-0983-0 | 87338-0983 |
| 87338-0983-00 | 87338-0983 |
| 87338-983-00 | 87338-983 |
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 |
|---|---|---|---|---|---|---|
| OpusMeds Extra Strength Minoxidil | MINOXIDIL | Opus Meds LLC | eab00b6d-d49a-4090-8243-ae5e99f6a54e | 2026-01-26 | Warnings | 87338-983-00 87338-983 87338098300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.