NDC11 00409230550
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 |
|---|---|
| 00409-2305-50 | 00409-2305 |
| 0409-2305-50 | 0409-2305 |
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 |
|---|---|---|---|---|---|---|
| MIDAZOLAM | MIDAZOLAM HYDROCHLORIDE | Hospira, Inc. | b95415fa-17c2-42ab-a6b0-e628d01c94ed | 2026-08-12 | Boxed warning, Warnings, Adverse reactions | 0409-2305-50 0409-2305 00409230550 |
| Midazolam | MIDAZOLAM HYDROCHLORIDE | Hospira, Inc. | 1abda8b8-48a8-4995-af86-39220d1aa240 | 2026-08-12 | Boxed warning, Warnings, Adverse reactions | 0409-2305 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.