NDC11 82725300203
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 |
|---|---|
| 82725-3002-03 | 82725-3002 |
| 82725-3002-3 | 82725-3002 |
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 |
|---|---|---|---|---|---|---|
| Cabinet Allergy Relief Fexofenadine | FEXOFENADINE HYDROCHLORIDE | Cabinet Health P.B.C. | 9ed710e1-47f4-4d04-a509-12c8c97c192c | 2025-11-05 | Warnings | 82725-3002 |
| Cabinet Allergy Relief Fexofenadine | FEXOFENADINE HYDROCHLORIDE | Cabinet Health P.B.C. | 5237c8bd-0b20-4639-a740-f3001c4c2c94 | 2025-10-22 | Warnings | 82725-3002-3 82725-3002 82725300203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.