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Last Updated: December 11, 2025

Details for New Drug Application (NDA): 211934

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NDA 211934 describes SODIUM NITROPRUSSIDE, which is a drug marketed by Abraxis Pharm, Amneal, Amphastar Pharms Inc, Avet Lifesciences, Baxter Hlthcare, Be Pharms, Caplin, Chartwell Rx, Cipla, Dr Reddys, Epic Pharma Llc, Eugia Pharma, Micro Labs, Mylan Labs Ltd, Nexus, Pharmobedient, Sagent Pharms Inc, Slate Run Pharma, Somerset Theraps Llc, Sun Pharm, Teva Parenteral, and Xiromed, and is included in twenty-three NDAs. It is available from fourteen suppliers. Additional details are available on the SODIUM NITROPRUSSIDE profile page.

The generic ingredient in SODIUM NITROPRUSSIDE is sodium nitroprusside. There are one thousand four hundred and seventy-two drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the sodium nitroprusside profile page.

Summary for 211934

Tradename:	SODIUM NITROPRUSSIDE
Applicant:	Eugia Pharma
Ingredient:	sodium nitroprusside
Patents:	0

Pharmacology for NDA: 211934

Physiological Effect	Vasodilation

Suppliers and Packaging for NDA: 211934

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
SODIUM NITROPRUSSIDE	sodium nitroprusside	INJECTABLE;INJECTION	211934	ANDA	AuroMedics Pharma LLC	55150-320	55150-320-01	1 VIAL, SINGLE-DOSE in 1 CARTON (55150-320-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	25MG/ML
Approval Date:	Dec 10, 2020	TE:		RLD:	No

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