Ifosfamide
Ifosfamide for Injection, USP
Approved
Approval ID
fb7f49af-ffe9-4969-a69c-8ed14dd0616b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 10, 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.
IFOSFAMIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63323-142
Application NumberANDA076078
Product Classification
M
Marketing Category
C73584
G
Generic Name
IFOSFAMIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 10, 2019
FDA Product Classification
INGREDIENTS (2)
BENZYL ALCOHOLInactive
Code: LKG8494WBH
Classification: IACT
IFOSFAMIDEActive
Quantity: 1 g in 1 1
Code: UM20QQM95Y
Classification: ACTIB