NDC11 00409329926
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 |
|---|---|
| 00409-3299-26 | 00409-3299 |
| 0409-3299-26 | 0409-3299 |
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 Acetate | SODIUM ACETATE | Hospira, Inc. | abc41ed1-9512-4bea-9295-1a9ca134b6c2 | 2026-03-26 | Warnings, Adverse reactions | 0409-3299 |
| Sodium Acetate | SODIUM ACETATE | Hospira, Inc. | c3be2468-45e8-4ecc-a30b-e966743a563f | 2026-03-26 | Warnings, Adverse reactions | 0409-3299-26 0409-3299 00409329926 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.