NDC11 00409729973
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 |
|---|---|
| 00409-7299-73 | 00409-7299 |
| 0409-7299-73 | 0409-7299 |
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. | ce9a7469-c4ba-4f60-8f7a-47ef0974316e | 2026-03-26 | Warnings, Adverse reactions | 0409-7299 |
| Sodium Acetate | SODIUM ACETATE | Hospira, Inc. | c91ede49-c7cc-47b7-0f93-e6841dd5916a | 2026-03-26 | Warnings, Adverse reactions | 0409-7299-73 0409-7299 00409729973 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.