NDC11 63304007801
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 |
|---|---|
| 63304-0078-01 | 63304-0078 |
| 63304-0078-1 | 63304-0078 |
| 63304-078-01 | 63304-078 |
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 | POTASSIUM CHLORIDE | Sun Pharmaceutical Industries, Inc. | 4d90d03d-7f0e-4d49-9e80-628dbc7165c0 | 2024-01-10 | Warnings, Adverse reactions | 63304-078-01 63304-078 63304007801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.