NDC11 00955105201
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 |
|---|---|
| 00955-1052-01 | 00955-1052 |
| 00955-1052-1 | 00955-1052 |
| 0955-1052-01 | 0955-1052 |
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 |
|---|---|---|---|---|---|---|
| Sevelamer Carbonate | SEVELAMER CARBONATE | Sanofi-Aventis U.S. LLC | 3abc32fe-1bfc-4759-8f7c-36095e221b06 | 2025-11-25 | Warnings, Adverse reactions | 0955-1052-01 0955-1052 00955105201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.