NDC11 10702003645
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 |
|---|---|
| 10702-0036-45 | 10702-0036 |
| 10702-036-45 | 10702-036 |
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 | KVK-Tech, Inc. | 905c3ee5-d1a7-4deb-a345-4a42296704fa | 2024-02-23 | Warnings, Adverse reactions | 10702-036-45 10702-036 10702003645 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.