NDCFind

Sodium Nitroprusside 70436-0028

Product NDC

70436-0028
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

IngredientStrength
Sodium Nitroprusside50 mg/2mL

Drug Class

Vasodilation [PE]Vasodilator [EPC]

Packaging Options(1)

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