NDC11 37835060209
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 |
|---|---|
| 37835-0602-09 | 37835-0602 |
| 37835-0602-9 | 37835-0602 |
| 37835-602-09 | 37835-602 |
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 | Bi-Mart | 0a3d4d1f-a99f-4d0a-bb28-b2409a9e073a | 2026-08-25 | Warnings | 37835-602-09 37835-602 37835060209 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.