Home > National Drug Code (NDC) > Fludarabine Phosphate

Fludarabine Phosphate - 0069-9321-22 - (Fludarabine Phosphate)

Alphabetical Index


Drug Information of Fludarabine Phosphate

Product NDC: 0069-9321
Proprietary Name: Fludarabine Phosphate
Non Proprietary Name: Fludarabine Phosphate
Active Ingredient(s): 25    mg/mL & nbsp;   Fludarabine Phosphate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fludarabine Phosphate

Product NDC: 0069-9321
Labeler Name: Pfizer Laboratories Div Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200647
Marketing Category: ANDA
Start Marketing Date: 20111222

Package Information of Fludarabine Phosphate

Package NDC: 0069-9321-22
Package Description: 2 mL in 1 VIAL (0069-9321-22)

NDC Information of Fludarabine Phosphate

NDC Code 0069-9321-22
Proprietary Name Fludarabine Phosphate
Package Description 2 mL in 1 VIAL (0069-9321-22)
Product NDC 0069-9321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fludarabine Phosphate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20111222
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer Inc.
Substance Name FLUDARABINE PHOSPHATE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of Fludarabine Phosphate


General Information