Sodium Nitroprusside
Sodium Nitroprusside Injection
Approved
Approval ID
5a689f89-3cbd-f9fa-13cc-26063feb9c83
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 19, 2019
Manufacturers
FDA
Dr.Reddy's Laboratories Inc.,
DUNS: 802315887
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 Code43598-587
Application NumberANDA210114
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sodium Nitroprusside
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 22, 2016
FDA Product Classification
INGREDIENTS (2)
WaterInactive
Code: 059QF0KO0R
Classification: IACT
Sodium NitroprussideActive
Quantity: 50 mg in 2 mL
Code: EAO03PE1TC
Classification: ACTIB