NDC11 65219051002
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 |
|---|---|
| 65219-0510-02 | 65219-0510 |
| 65219-0510-2 | 65219-0510 |
| 65219-510-02 | 65219-510 |
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 Acetate | POTASSIUM ACETATE | Fresenius Kabi USA, LLC | bf4dc488-d6f3-41f8-ac8d-37b27f25b8db | 2024-12-06 | Warnings, Adverse reactions | 65219-510-02 65219-510 65219051002 |