MedPath

Sodium Nitroprusside

Approved
Approval ID

a8c5d04b-c6cb-46e6-b90c-e858a0a52406

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 5, 2019

Manufacturers
FDA

Caplin Steriles Limited

DUNS: 650744670

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Sodium Nitroprusside

PRODUCT DETAILS

NDC Product Code65145-101
Application NumberANDA211016
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateNovember 29, 2017
Generic NameSodium Nitroprusside

INGREDIENTS (2)

SODIUM NITROPRUSSIDEActive
Quantity: 50 mg in 2 mL
Code: EAO03PE1TC
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Sodium Nitroprusside - FDA Drug Approval Details