NDC11 00409409301
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 |
|---|---|
| 00409-4093-01 | 00409-4093 |
| 00409-4093-1 | 00409-4093 |
| 0409-4093-01 | 0409-4093 |
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 |
|---|---|---|---|---|---|---|
| CHROMIUM | CHROMIC CHLORIDE | Hospira, Inc. | b4d01ebb-a36e-44b7-028c-43c0ab2d13b4 | 2026-06-24 | Warnings, Adverse reactions | 0409-4093-01 0409-4093 00409409301 |
| Chromium | CHROMIC CHLORIDE | Hospira, Inc. | da207ca8-7836-4c66-92fe-36cc89baf773 | 2026-06-24 | Warnings, Adverse reactions | 0409-4093 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.