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Fludarabine Phosphate - 61703-344-18 - (FLUDARABINE PHOSPHATE)

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Drug Information of Fludarabine Phosphate

Product NDC: 61703-344
Proprietary Name: Fludarabine Phosphate
Non Proprietary Name: FLUDARABINE PHOSPHATE
Active Ingredient(s): 50    mg/2mL & nbsp;   FLUDARABINE PHOSPHATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fludarabine Phosphate

Product NDC: 61703-344
Labeler Name: Hospira Worldwide, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077790
Marketing Category: ANDA
Start Marketing Date: 20070406

Package Information of Fludarabine Phosphate

Package NDC: 61703-344-18
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-344-18) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Fludarabine Phosphate

NDC Code 61703-344-18
Proprietary Name Fludarabine Phosphate
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-344-18) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 61703-344
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FLUDARABINE PHOSPHATE
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070406
Marketing Category Name ANDA
Labeler Name Hospira Worldwide, Inc.
Substance Name FLUDARABINE PHOSPHATE
Strength Number 50
Strength Unit mg/2mL
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of Fludarabine Phosphate


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