NDC11 00603155404
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 |
|---|---|
| 00603-1554-04 | 00603-1554 |
| 00603-1554-4 | 00603-1554 |
| 0603-1554-04 | 0603-1554 |
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 | Endo USA, Inc. | a64d7151-09a6-474c-83fc-36c7cf582d32 | 2025-03-26 | Warnings, Adverse reactions | 0603-1554-04 0603-1554 00603155404 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.