NDC11 80425023201
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 |
|---|---|
| 80425-0232-01 | 80425-0232 |
| 80425-0232-1 | 80425-0232 |
| 80425-232-01 | 80425-232 |
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 |
|---|---|---|---|---|---|---|
| DoubleDex Kit | DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE | Advanced Rx Pharmacy of Tennessee, LLC | fb85dd2c-6c90-6249-e053-6294a90a09fa | 2024-12-31 | Warnings, Adverse reactions | 80425-0232-1 80425-0232 80425023201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.