NDC11 13517010030
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 |
|---|---|
| 13517-0100-30 | 13517-0100 |
| 13517-100-30 | 13517-100 |
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 |
|---|---|---|---|---|---|---|
| Diazoxide | DIAZOXIDE | e5 Pharma, LLC | c0237320-2d3f-4907-a4d3-08f138aa4ca8 | 2025-07-31 | Warnings, Adverse reactions | 13517-100-30 13517-100 13517010030 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.