Sodium Nitroprusside 71839-0120
Product NDC
71839-0120- Manufacturer
- Be Pharmaceuticals Inc.
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 12, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA214971
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Nitroprusside | 50 mg/2mL |
Drug Class
Vasodilation [PE]Vasodilator [EPC]
Packaging Options(1)
1 VIAL in 1 CARTON (71839-120-01) / 2 mL in 1 VIAL