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FDA shortage status: Ifosfamide Injection

FDA shortage status · Source checked 2026-10-06T18:55:41+00:00

FDA source answer

FDA currently lists this ingredient in shortage.

FDA source statuses: Current. First FDA posting: 2026-06-12. Latest FDA row update: 2026-10-02.

FDA lists 8 package records, with companies: Baxter Healthcare, Baxter Healthcare Company, Baxter Healthcare Corporation, Fresenius Kabi USA, LLC, Hikma Pharmaceuticals USA Inc., Hikma Pharmaceuticals USA, Inc., SteriMax Inc., SteriMax, Inc.. Package NDCs: 0143-9530-01, 0143-9531-01, 0338-3991-01, 0338-3993-01, 10019-925-01, 10019-926-02, 21586-211-02, 63323-142-10.

FDA shortage reason: Demand increase for the drug; Requirements related to complying with good manufacturing practices

This is nationwide FDA status, not local pharmacy inventory. CiteFacts does not provide medical, treatment, substitution, or dosing advice.

FDA package and manufacturer records

CompanyPackage NDCPresentationFDA availability fieldFDA update
Baxter Healthcare0338-3991-01IFEX, Injection, 1 g/20 mL (NDC 0338-3991-01)Available2026-10-02
Baxter Healthcare0338-3993-01IFEX, Injection, 3 g/60 mL (NDC 0338-3993-01)Unavailable2026-10-02
Baxter Healthcare10019-925-01Ifosfamide, Injection, 1 g/20 mL (NDC 10019-925-01)Available2026-10-02
Baxter Healthcare10019-926-02Ifosfamide, Injection, 3 g/60 mL (NDC 10019-926-02)Available2026-10-02
Fresenius Kabi USA, LLC63323-142-10Ifosfamide, Injection, 1 g/1 (NDC 63323-142-10)Limited Availability2026-09-15
Hikma Pharmaceuticals USA, Inc.0143-9530-01Ifosfamide, Injection, 50 mg/1 mL (NDC 0143-9530-01)Unavailable2026-09-18
Hikma Pharmaceuticals USA, Inc.0143-9531-01Ifosfamide, Injection, 50 mg/1 mL (NDC 0143-9531-01)Unavailable2026-09-18
SteriMax, Inc.21586-211-02Ifosfamide, Injection, 1 g/1 (NDC 21586-211-02)Available2026-09-08

Source facts

Grouped generic ingredient: Ifosfamide Injection · 8 package records

Therapeutic categories: Oncology, Pediatric
Dosage forms: Injection
Routes: INTRAVENOUS

Open FDA source data · JSON · Markdown

FDA is authoritative. Source retrieved 2026-10-06T18:55:41+00:00. Derived grouping is documented in this record's derivations.