NDC 0703-3427

Ifosfamide

Ifosfamide

Ifosfamide is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Teva Parenteral Medicines, Inc.. The primary component is Ifosfamide.

Product ID0703-3427_5cc5463c-26b4-4163-9968-e7f692d1c253
NDC0703-3427
Product TypeHuman Prescription Drug
Proprietary NameIfosfamide
Generic NameIfosfamide
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2007-07-26
Marketing CategoryANDA / ANDA
Application NumberANDA076657
Labeler NameTeva Parenteral Medicines, Inc.
Substance NameIFOSFAMIDE
Active Ingredient Strength1 g/20mL
Pharm ClassesAlkylating Activity [MoA],Alkylating Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0703-3427-11

1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3427-11) > 20 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date2007-07-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0703-3427-11 [00703342711]

Ifosfamide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA076657
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2007-07-26

Drug Details

Active Ingredients

IngredientStrength
IFOSFAMIDE1 g/20mL

OpenFDA Data

SPL SET ID:14f535d7-4593-4cee-94fb-54ee239d95d2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1791599
  • 1791597

    • Pharmacological Class

    • Alkylating Activity [MoA]
    • Alkylating Drug [EPC]

    NDC Crossover Matching brand name "Ifosfamide" or generic name "Ifosfamide"

    NDCBrand NameGeneric Name
    0143-9530IfosfamideIfosfamide
    0143-9531IfosfamideIfosfamide
    0703-3427IfosfamideIfosfamide
    0703-3429IfosfamideIfosfamide
    10019-925IFOSFAMIDEIFOSFAMIDE
    10019-926IFOSFAMIDEIFOSFAMIDE
    10019-927IFOSFAMIDEifosfamide
    10019-929IFOSFAMIDEifosfamide
    63323-142IfosfamideIFOSFAMIDE
    0338-3991IFEXifosfamide
    0338-3993IFEXifosfamide
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