sodium nitroprusside
Sodium Nitroprusside Injection
Approved
Approval ID
870b8428-3e48-40f5-9172-d962adc90dd5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 9, 2022
Manufacturers
FDA
Nexus Pharmaceuticals Inc
DUNS: 620714787
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 Code14789-012
Application NumberANDA207499
Product Classification
M
Marketing Category
C73584
G
Generic Name
sodium nitroprusside
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 9, 2022
FDA Product Classification
INGREDIENTS (2)
sodium nitroprussideActive
Quantity: 25 mg in 1 mL
Code: EAO03PE1TC
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT