United States · FDA National Drug Code directory

IFEX

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0338-3993_56f50d8e-7c87-4119-a7dc-bfd77fa3dcec
Product NDC
0338-3993
Form
INJECTION, POWDER, FOR SOLUTION
Composition / generic term
ifosfamide
Labeler
Baxter Healthcare Corporation
Marketing category
NDA
Marketing start / end (source format)
19881230
Source listing expiry
20271231

Source-listed ingredients

  • IFOSFAMIDE — 3 g/60mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0338-3993-01) / 60 mL in 1 VIAL, SINGLE-DOSE · 0338-3993-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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