Ifosfamide (Fresenius Kabi USA, LLC)


Welcome to the PulseAid listing for the Ifosfamide drug offered from Fresenius Kabi USA, LLC. This Alkylating Activity [MoA],Alkylating Drug [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Fresenius Kabi USA, LLC
NON-PROPRIETARY NAME: IFOSFAMIDE
SUBSTANCE NAME: IFOSFAMIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Alkylating Activity [MoA],Alkylating Drug [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2003-01-28
END MARKETING DATE: 0000-00-00


Ifosfamide HUMAN PRESCRIPTION DRUG Details:

Item DescriptionIfosfamide from Fresenius Kabi USA, LLC
LABELER NAME: Fresenius Kabi USA, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1(g/1)
START MARKETING DATE: 2003-01-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63323-142_4c63407f-1190-43b8-9ce8-6d17042874f6
PRODUCT NDC: 63323-142
APPLICATION NUMBER: ANDA076078

Other IFOSFAMIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
APP Pharmaceuticals, LLCIfosfamide
Baxter Healthcare CorporationIFEX
Fresenius Kabi USA, LLCIfosfamide
Mylan Institutional LLCIfosfamide
Pfizer Laboratories Div Pfizer Inc.Ifosfamide
Teva Parenteral Medicines, Inc.Ifosfamide
West-Ward Pharmaceuticals CorpIfosfamide