Ifosfamide - 63323-174-60 - (IFOSFAMIDE)

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Drug Information of Ifosfamide

Product NDC: 63323-174
Proprietary Name: Ifosfamide
Non Proprietary Name: IFOSFAMIDE
Active Ingredient(s): 50    mg/mL & nbsp;   IFOSFAMIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ifosfamide

Product NDC: 63323-174
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090181
Marketing Category: ANDA
Start Marketing Date: 20090930

Package Information of Ifosfamide

Package NDC: 63323-174-60
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-174-60) > 60 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Ifosfamide

NDC Code 63323-174-60
Proprietary Name Ifosfamide
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-174-60) > 60 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-174
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name IFOSFAMIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090930
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name IFOSFAMIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of Ifosfamide


General Information