Application Information

This drug has been submitted to the FDA under the reference 209387/001.

Names and composition

"NIPRIDE RTU IN SODIUM CHLORIDE 0.9%" is the commercial name of a drug composed of SODIUM NITROPRUSSIDE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
209387/001 NIPRIDE RTU IN SODIUM CHLORIDE 0.9% SODIUM NITROPRUSSIDE SOLUTION/IV (INFUSION) 50MG per 100ML (0.5MG per ML)

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
017546/001 NIPRIDE SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 50MG per VIAL
018450/001 NITROPRESS SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 50MG per VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
018581/001 SODIUM NITROPRUSSIDE SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 50MG per VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
070031/001 SODIUM NITROPRUSSIDE SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 50MG per VIAL
070566/001 NITROPRESS SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 50MG per VIAL
071555/001 NITROPRESS SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 50MG per VIAL
071961/001 NITROPRESS SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 25MG per ML
073465/001 SODIUM NITROPRUSSIDE SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 25MG per ML
207426/001 SODIUM NITROPRUSSIDE SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 25MG per ML
207499/001 SODIUM NITROPRUSSIDE SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 25MG per ML
208635/001 SODIUM NITROPRUSSIDE SODIUM NITROPRUSSIDE INJECTABLE/INJECTION 25MG per ML
209387/001 NIPRIDE RTU IN SODIUM CHLORIDE 0.9% SODIUM NITROPRUSSIDE SOLUTION/IV (INFUSION) 50MG per 100ML (0.5MG per ML)

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