NDC11 60687063201
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 |
|---|---|
| 60687-0632-01 | 60687-0632 |
| 60687-0632-1 | 60687-0632 |
| 60687-632-01 | 60687-632 |
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 |
|---|---|---|---|---|---|---|
| Potassium Chloride Extended-Release | POTASSIUM CHLORIDE | American Health Packaging | 8c12c5f8-5950-44e3-9473-a0b95187b43c | 2024-08-22 | Warnings, Adverse reactions | 60687-632-01 60687-632 60687063201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.