NDC11 00338019204
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 |
|---|---|
| 00338-0192-04 | 00338-0192 |
| 00338-0192-4 | 00338-0192 |
| 00338-192-04 | 00338-192 |
| 0338-0192-04 | 0338-0192 |
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 |
|---|---|---|---|---|---|---|
| Sodium Chloride | SODIUM CHLORIDE | Baxter Healthcare Corporation | 2fae04e3-20b1-4b8c-b1fb-646b384836f1 | 2022-12-07 | Warnings, Adverse reactions | 0338-0192-04 0338-0192 00338019204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.