Ifosfamide - 55390-048-01 - (Ifosfamide)

Alphabetical Index


Drug Information of Ifosfamide

Product NDC: 55390-048
Proprietary Name: Ifosfamide
Non Proprietary Name: Ifosfamide
Active Ingredient(s): 50    mg/mL & nbsp;   Ifosfamide
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ifosfamide

Product NDC: 55390-048
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076619
Marketing Category: ANDA
Start Marketing Date: 20100831

Package Information of Ifosfamide

Package NDC: 55390-048-01
Package Description: 1 VIAL, SINGLE-DOSE in 1 BOX (55390-048-01) > 60 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Ifosfamide

NDC Code 55390-048-01
Proprietary Name Ifosfamide
Package Description 1 VIAL, SINGLE-DOSE in 1 BOX (55390-048-01) > 60 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55390-048
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ifosfamide
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20100831
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name IFOSFAMIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of Ifosfamide


General Information