Diazoxide
- Product NDC
- 0254-1010
- 11-digit product format
- 002541010
- Labeler code
- 0254
- Product ID
- 0254-1010_ca21c9b7-669a-4f0f-afe0-0b166c13bb98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazoxide
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Par Health USA, LLC
- Application
- ANDA210799
- Marketing category
- ANDA
- Marketing start
- 2020-07-21
- Substance
- DIAZOXIDE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Diazoxide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIAZOXIDE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O5CB12L4FN |
| Rxcui | 197593 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0254-1010-19 | Diazoxide | 30 mL in 1 BOTTLE, DROPPER | SUSPENSION | 30 | | 7 |
| 0254-1010-19 | Diazoxide | 1 in 1 CARTON | SUSPENSION | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0254-1010 | DIAZOXIDE SUSPENSION [ENDO USA, INC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20240913_abe317a5-6c63-469c-89c8-9fedfe859c3d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0254-1010-19 | 00254101019 | 1 BOTTLE, DROPPER in 1 CARTON (0254-1010-19) / 30 mL in 1 BOTTLE, DROPPER | 2020-07-21 | 0000-00-00 | No | No | Current |