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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code65145-101
Application NumberANDA211016
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sodium Nitroprusside
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateNovember 29, 2017
FDA Product Classification
INGREDIENTS (2)
SODIUM NITROPRUSSIDEActive
Quantity: 50 mg in 2 mL
Code: EAO03PE1TC
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT