NDC11 73581021002
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 |
|---|---|
| 73581-0210-02 | 73581-0210 |
| 73581-0210-2 | 73581-0210 |
| 73581-210-02 | 73581-210 |
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 |
|---|---|---|---|---|---|---|
| Butenafine Hydrochloride | BUTENAFINE HYDROCHLORIDE | YYBA CORP | e650d8aa-c809-42ee-a1d9-a6321d5364f5 | 2025-12-10 | Warnings | 73581-210-02 73581-210 73581021002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.