Sodium Nitroprusside
Sodium Nitroprusside InjectionRx only
Approved
Approval ID
2122b9c1-0af4-493b-82cc-63eee02f987f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 14, 2023
Manufacturers
FDA
Somerset Therapeutics, LLC
DUNS: 079947873
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 Code70069-261
Application NumberANDA210882
Product Classification
M
Marketing Category
C73584
G
Generic Name
Sodium Nitroprusside
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 14, 2023
FDA Product Classification
INGREDIENTS (2)
SODIUM NITROPRUSSIDEActive
Quantity: 25 mg in 1 mL
Code: EAO03PE1TC
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT