Sodium Nitroprusside 70069-0261-01

Package NDC

70069-0261-01

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]

Selected Package

70069-0261-01Selected

1 VIAL in 1 CARTON (70069-261-01) / 2 mL in 1 VIAL