NDC11 84324000802
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 |
|---|---|
| 84324-0008-02 | 84324-0008 |
| 84324-0008-2 | 84324-0008 |
| 84324-008-02 | 84324-008 |
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 HYDROCHLORIDE | FEXOFENADINE HYDROCHLORIDE | NUVICARE LLC | bb47b839-3f49-4818-a62c-b6d2b09b15dc | 2025-12-19 | Warnings | 84324-008 |
| FEXOFENADINE HYDROCHLORIDE | FEXOFENADINE HYDROCHLORIDE | NUVICARE LLC | ec55732c-a3db-4445-a06d-0f98b21ed134 | 2025-06-09 | Warnings | 84324-008-02 84324-008 84324000802 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.