Floxuridine
Floxuridine for Injection, USP
Approved
Approval ID
c8edabc1-67cd-421b-a147-7c1f19f05b8e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 31, 2019
Manufacturers
FDA
Fresenius Kabi USA, LLC
DUNS: 608775388
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
FLOXURIDINE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63323-145
Application NumberANDA075837
Product Classification
M
Marketing Category
C73584
G
Generic Name
FLOXURIDINE
Product Specifications
Route of AdministrationINTRA-ARTERIAL
Effective DateDecember 31, 2019
FDA Product Classification
INGREDIENTS (1)
FLOXURIDINEActive
Quantity: 500 mg in 5 mL
Code: 039LU44I5M
Classification: ACTIB