NDC11 37808039102
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 |
|---|---|
| 37808-0391-02 | 37808-0391 |
| 37808-0391-2 | 37808-0391 |
| 37808-391-02 | 37808-391 |
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 |
|---|---|---|---|---|---|---|
| Allergy Relief | FEXOFENADINE HYDROCHLORIDE | HEB | 7cb25829-3aee-4a82-869d-ab4259626584 | 2022-05-31 | Warnings | 37808-391-02 37808-391 37808039102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.