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Fludarabine Phosphate - 67457-238-02 - (Fludarabine Phosphate)

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Drug Information of Fludarabine Phosphate

Product NDC: 67457-238
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fludarabine Phosphate

Product NDC: 67457-238
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090724
Marketing Category: ANDA
Start Marketing Date: 20130130

Package Information of Fludarabine Phosphate

Package NDC: 67457-238-02
Package Description: 1 VIAL, GLASS in 1 CARTON (67457-238-02) > 2 mL in 1 VIAL, GLASS

NDC Information of Fludarabine Phosphate

NDC Code 67457-238-02
Proprietary Name Fludarabine Phosphate
Package Description 1 VIAL, GLASS in 1 CARTON (67457-238-02) > 2 mL in 1 VIAL, GLASS
Product NDC 67457-238
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fludarabine Phosphate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130130
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
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


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