NDC11 46287000601
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 |
|---|---|
| 46287-0006-01 | 46287-0006 |
| 46287-0006-1 | 46287-0006 |
| 46287-006-01 | 46287-006 |
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 | CMP Pharma, Inc. | 12d48dcf-07bd-4b06-bd6c-7543f1be8357 | 2021-08-15 | Warnings, Adverse reactions | 46287-006-01 46287-006 46287000601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.