Sodium Nitroprusside 70436-0028-80

Package NDC

70436-0028-80

Manufacturer: Slate Run Pharmaceuticals, Llc
Dosage Form: Injection, Solution, Concentrate
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: October 15, 2020
Listing Expires: December 31, 2026
Application: ANDA214199

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Active Ingredients

Ingredient	Strength
Sodium Nitroprusside	50 mg/2mL

Drug Class

Vasodilation [PE]Vasodilator [EPC]

Selected Package

70436-0028-80Selected

1 VIAL in 1 CARTON (70436-028-80) / 2 mL in 1 VIAL