Home > National Drug Code (NDC) > Fludarabine Phosphate

Fludarabine Phosphate - 0703-4852-11 - (Fludarabine Phosphate)

Alphabetical Index


Drug Information of Fludarabine Phosphate

Product NDC: 0703-4852
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: 0703-4852
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076661
Marketing Category: ANDA
Start Marketing Date: 20040428

Package Information of Fludarabine Phosphate

Package NDC: 0703-4852-11
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-4852-11) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Fludarabine Phosphate

NDC Code 0703-4852-11
Proprietary Name Fludarabine Phosphate
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-4852-11) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0703-4852
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fludarabine Phosphate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20040428
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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