NDC11 68001061900
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 |
|---|---|
| 68001-0619-0 | 68001-0619 |
| 68001-0619-00 | 68001-0619 |
| 68001-619-00 | 68001-619 |
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 | BluePoint Laboratories | 3709ee9a-f885-4a75-ab51-36e9e1ef0427 | 2025-11-10 | Warnings, Adverse reactions | 68001-619-00 68001-619 68001061900 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.