WARFARIN SODIUM
WARFARIN SODIUM
Approved
Approval ID
c60374ce-2338-4026-8c7c-5295934dce17
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 23, 2015
Manufacturers
FDA
Northwind Pharmaceuticals, LLC
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
WARFARIN SODIUM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51655-282
Application NumberANDA040663
Product Classification
M
Marketing Category
C73584
G
Generic Name
WARFARIN SODIUM
Product Specifications
Route of AdministrationORAL
Effective DateMarch 23, 2015
FDA Product Classification
INGREDIENTS (1)
WARFARIN SODIUMActive
Quantity: 4 mg in 1 1
Code: 6153CWM0CL
Classification: ACTIB