Diazoxide Oral Solution
- Product NDC
- 80432-057
- 11-digit product format
- 804320057
- Labeler code
- 80432
- Product ID
- 80432-057_f1863e5d-f2b6-2e47-e053-2a95a90af475
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazoxide Oral Suspension
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- TriRx Huntsville Pharmaceutical Services LLC
- Application
- ANDA211050
- Marketing category
- ANDA
- Marketing start
- 2023-01-06
- Marketing end
- 0000-00-00
- Substance
- DIAZOXIDE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80432-057-06 | 80432005706 | 1 BOTTLE, DROPPER in 1 CARTON (80432-057-06) > 30 mL in 1 BOTTLE, DROPPER | 2023-01-06 | 0000-00-00 | No | No | Current |