NDC11 21586021102

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
21586-0211-02	21586-0211
21586-0211-2	21586-0211
21586-211-02	21586-211

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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ifosfamide	IFOSFAMIDE FOR INJECTION	SteriMax Inc.	98798c5e-8384-4990-a1b5-60dfb1e667bb	2026-09-01		Exact identifier ndc (package): 21586-211-02 ndc (product): 21586-211 ndc11 (package): 21586021102

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.