NDC11 37835060109
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 |
|---|---|
| 37835-0601-09 | 37835-0601 |
| 37835-0601-9 | 37835-0601 |
| 37835-601-09 | 37835-601 |
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 HCL | Bi-Mart | ea8d8e12-4781-4501-a887-e732295d33bf | 2025-04-28 | Warnings | 37835-601-09 37835-601 37835060109 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.