Search by Drug Name or NDC

NDC 00338-3991-01 IFEX 1 g/20mL Details

IFEX 1 g/20mL

IFEX is a INTRAVENOUS INJECTION, POWDER, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is IFOSFAMIDE.

MedlinePlus Drug Summary

Ifosfamide is used in combination with other medications to treat cancer of the testicles that has not improved or that has worsened after treatment with other medications or radiation therapy. Ifosfamide is in a class of medications called alkylating agents. It works by slowing or stopping the growth of cancer cells in your body.

Related Packages: 00338-3991-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ifosfamide Injection

Product Information

NDC	00338-3991
Product ID	0338-3991_8f059d89-8848-4f29-aa9a-d14a4721df47
Associated GPIs	21101025002110
GCN Sequence Number	016500
GCN Sequence Number Description	ifosfamide VIAL 1 G INTRAVEN
HIC3	V1A
HIC3 Description	ANTINEOPLASTIC - ALKYLATING AGENTS
GCN	48862
HICL Sequence Number	004570
HICL Sequence Number Description	IFOSFAMIDE
Brand/Generic	Brand
Proprietary Name	IFEX
Proprietary Name Suffix	n/a
Non-Proprietary Name	ifosfamide
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	INJECTION, POWDER, FOR SOLUTION
Route	INTRAVENOUS
Active Ingredient Strength	1
Active Ingredient Units	g/20mL
Substance Name	IFOSFAMIDE
Labeler Name	Baxter Healthcare Corporation
Pharmaceutical Class	Alkylating Activity [MoA], Alkylating Drug [EPC]
DEA Schedule	n/a
Marketing Category	NDA
Application Number	NDA019763
Listing Certified Through	2024-12-31

Package

NDC 00338-3991-01 (00338399101)

Pricing Information	N/A
NDC Package Code	0338-3991-01
Billing NDC	00338399101
Package	1 VIAL, SINGLE-DOSE in 1 CARTON (0338-3991-01) / 20 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date	1988-12-30
NDC Exclude Flag	N