NDC11 84549035201
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 |
|---|---|
| 84549-0352-01 | 84549-0352 |
| 84549-0352-1 | 84549-0352 |
| 84549-352-01 | 84549-352 |
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 | SODIUM BICARBONATE | ProPharma Distribution | 3d71b046-3e0b-054a-e063-6294a90a563a | 2025-08-28 | Warnings, Adverse reactions | 84549-352-01 84549-352 84549035201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.