NDC11 00409601025
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 |
|---|---|
| 00409-6010-25 | 00409-6010 |
| 0409-6010-25 | 0409-6010 |
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 |
|---|---|---|---|---|---|---|
| PROPOFOL | PROPOFOL | Hospira, Inc. | 28d7ba00-f824-4e55-139a-03f509c099db | 2026-08-13 | Warnings, Adverse reactions | 0409-6010-25 0409-6010 00409601025 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.