NDC11 72090001099
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 |
|---|---|
| 72090-0010-99 | 72090-0010 |
| 72090-010-99 | 72090-010 |
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 | Pioneer Life Sciences, LLC | d7fe71e4-aada-40f5-86a8-bf0d7eb9b851 | 2025-12-26 | Warnings | 72090-010 |
| FEXOFENADINE HYDROCHLORIDE | FEXOFENADINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | 0a4f4178-bea5-4995-99dc-96980cccdc8a | 2025-12-26 | Warnings | 72090-010 |
| FEXOFENADINE HYDROCHLORIDE | FEXOFENADINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | d3b6f04c-60d6-4ac3-9fb2-19eeb80f00a5 | 2025-06-01 | Warnings | 72090-010-99 72090-010 72090001099 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.