Sodium Nitroprusside 70069-0261
Product NDC
70069-0261- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- August 17, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210882
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Nitroprusside | 25 mg/mL |
Drug Class
Vasodilation [PE]Vasodilator [EPC]
Packaging Options(1)
1 VIAL in 1 CARTON (70069-261-01) / 2 mL in 1 VIAL