NDC11 35573010814
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 |
|---|---|
| 35573-0108-14 | 35573-0108 |
| 35573-108-14 | 35573-108 |
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 |
|---|---|---|---|---|---|---|
| Sodium Polystyrene Sulfonate | SODIUM POLYSTYRENE SULFONATE | Burel Pharmaceuticals, LLC | 8bbeae67-a7ff-4fa6-b21e-fb8617cd9197 | 2025-05-01 | Warnings, Adverse reactions | 35573-108-14 35573-108 35573010814 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.