Sodium Nitroprusside 71839-0120-01

Package NDC

71839-0120-01

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]

Selected Package

71839-0120-01Selected

1 VIAL in 1 CARTON (71839-120-01) / 2 mL in 1 VIAL