NDC11 76045020400
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 |
|---|---|
| 76045-0204-0 | 76045-0204 |
| 76045-0204-00 | 76045-0204 |
| 76045-204-00 | 76045-204 |
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 |
|---|---|---|---|---|---|---|
| Diazepam | DIAZEPAM | Fresenius Kabi USA, LLC | ae52866a-0b9a-4baf-af1b-f9d5e00c0e56 | 2025-08-07 | Boxed warning, Warnings, Adverse reactions | 76045-204-00 76045-204 76045020400 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.