NDC 73377-056 - Diazoxide
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 73377-056
- Package NDCs from labels
- 73377-056-01, 73377-056-02, 73377-056-03
- Manufacturer
- AX Pharmaceutical Corp
- Effective date
- 2020-08-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diazoxide - AX Pharmaceutical Corp | AX Pharmaceutical Corp | 2020-08-18 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73377-056-01 | Diazoxide | 500 g in 1 JAR | POWDER | 500 | 3 | |
| 73377-056-02 | Diazoxide | 1000 g in 1 JAR | POWDER | 1000 | 3 | |
| 73377-056-03 | Diazoxide | 100 g in 1 JAR | POWDER | 100 | 3 |
DailyMed Dashboard NDC Coverage#
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 | Par Health USA, LLC | abe317a5-6c63-469c-89c8-9fedfe859c3d | 2026-08-07 | Warnings, Adverse reactions | O5CB12L4FN |
| Diazoxide | DIAZOXIDE | e5 Pharma, LLC | c0237320-2d3f-4907-a4d3-08f138aa4ca8 | 2025-07-31 | Warnings, Adverse reactions | O5CB12L4FN |
| Proglycem | DIAZOXIDE | Teva Pharmaceuticals USA, Inc. | b16c7832-2fd9-49af-b923-1dc0d91fd6e2 | 2024-07-19 | Warnings, Adverse reactions | O5CB12L4FN |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.