Home NDC 21586-211 Ifosfamide
Product NDC 21586-211
11-digit product format 215860211
Labeler code 21586
Product ID 21586-211_28dd8f2a-6b41-4b8b-bb70-23fe0b58c665
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ifosfamide for Injection
Dosage form POWDER, FOR SOLUTION
Route INTRAVENOUS
Labeler SteriMax Inc.
Marketing category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start 2026-09-04
Substance IFOSFAMIDE
Active strength 1 g/1
Pharmacologic classes Alkylating Activity [MoA], Alkylating Drug [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ifosfamide
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IFOSFAMIDE 1 g/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination UM20QQM95Y Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1791593 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 21586-211-02 21586021102 5 VIAL in 1 CARTON (21586-211-02) / 1 POWDER, FOR SOLUTION in 1 VIAL (21586-211-01) 5 vial 2026-09-04 No No Current