NDC11 73581001202
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 |
|---|---|
| 73581-0012-02 | 73581-0012 |
| 73581-0012-2 | 73581-0012 |
| 73581-012-02 | 73581-012 |
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 |
|---|---|---|---|---|---|---|
| Fexofenadine | FEXOFENADINE | YYBA Corp | 579c7ff9-0c44-1d46-e063-6294a90aef34 | 2026-07-27 | Warnings | 73581-012-02 73581-012 73581001202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.