NDC11 80513061102
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 |
|---|---|
| 80513-0611-02 | 80513-0611 |
| 80513-0611-2 | 80513-0611 |
| 80513-611-02 | 80513-611 |
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 Bicarbonate 10 GR (650 MG) | SODIUM BICARBONATE | Advanced Rx LLC | 634e8d52-6d04-42f9-98f6-2634473b5dfd | 2025-09-01 | Warnings | 80513-611-02 80513-611 80513061102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.