NDC11 54973523001
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 |
|---|---|
| 54973-5230-01 | 54973-5230 |
| 54973-5230-1 | 54973-5230 |
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 |
|---|---|---|---|---|---|---|
| KALI SULPH | POTASSIUM SULFATE | Hyland's Inc. | c00e31d8-76df-47b1-bafd-36d088395522 | 2022-12-19 | Warnings | 54973-5230-1 54973-5230 54973523001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.