Fludarabine (Fresenius Kabi USA, LLC)


Welcome to the PulseAid listing for the Fludarabine drug offered from Fresenius Kabi USA, LLC. This Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [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: FLUDARABINE PHOSPHATE
SUBSTANCE NAME: FLUDARABINE PHOSPHATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2007-11-16
END MARKETING DATE: 0000-00-00


Fludarabine HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFludarabine from Fresenius Kabi USA, LLC
LABELER NAME: Fresenius Kabi USA, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 25(mg/mL)
START MARKETING DATE: 2007-11-16
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63323-192_40c40275-b5a2-4682-9c89-f92f55bb05fb
PRODUCT NDC: 63323-192
APPLICATION NUMBER: ANDA078393

Other FLUDARABINE PHOSPHATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actavis Pharma, Inc.Fludarabine phosphate
APP Pharmaceuticals, LLCFludarabine
Fresenius Kabi USA, LLCFludarabine
Hospira, Inc.Fludarabine Phosphate
Mylan Institutional LLCFludarabine Phosphate
Pfizer Laboratories Div Pfizer Inc.Fludarabine Phosphate
Sagent PharmaceuticalsFludarabine Phosphate
Sandoz IncFludarabine Phosphate
Teva Parenteral Medicines, Inc.Fludarabine Phosphate