NDC11 69945060220

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
69945-0602-20	69945-0602
69945-602-20	69945-602

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
SODIUM IODIDE I 123	SODIUM IODIDE I 123	Curium US LLC	493fa2ab-4eb0-4434-9739-3079b2f0e272	2024-10-17	Warnings, Adverse reactions	Exact identifier ndc (package): 69945-602-20 ndc (product): 69945-602 ndc11 (package): 69945060220

Reported adverse events (FAERS/openFDA)#

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